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Genetics and genomics
Research
Fabry disease due to D313Y and novel GLA mutations
  1. Konstantinos Koulousios1,
  2. Konstantinos Stylianou2,
  3. Panagiotis Pateinakis3,
  4. Maria Zamanakou4,
  5. Gedeon Loules4,
  6. Eleni Manou3,
  7. Parthena Kyriklidou3,
  8. Christos Katsinas5,
  9. Alexandra Ouzouni6,
  10. John Kyriazis7,
  11. Matthaios Speletas1,
  12. Anastasios E Germenis1
  1. 1 Department of Immunology & Histocompatibility, School of Medicine, University of Thessaly, Larissa, Greece
  2. 2 University Hospital of Heraklion, Heraklion, Greece
  3. 3 Papageorgiou General Hospital, Thessaloniki, Greece
  4. 4 CeMIA SA, Larissa, Greece
  5. 5 Mpodosakeio General Hospital, Ptolemaida, Greece
  6. 6 Kavala General Hospital, Kavala, Greece
  7. 7 Chios General Hospital, Chios, Greece
  1. Correspondence to Konstantinos Koulousios; konkoul{at}gmail.com

Abstract

Objectives Our aim is to report four novel α-gal A gene (GLA) mutations resulting in Fabry disease (FD) and provide evidence of pathogenicity of the D313Y mutation regarding which contradictory data have been presented in the literature.

Setting and participants Twenty-five family members of nine unrelated patients with definite FD diagnosis, 10 clinically suspected cases and 18 members of their families were included in this polycentric cohort study.

Primary and secondary outcome measures Genotyping and measurement of lyso-Gb3 was performed in all individuals. The α-Gal A activity was measured in all men as well as plasma and urine Gb3 concentration in selected cases. Optical and electron microscopy was performed in kidney biopsies of selected patients. All the above were evaluated in parallel with the clinical data of the patients.

Results Fourteen new cases of FD were recognised, four of which were carrying already described GLA mutations. Four novel GLA mutations, namely c.835C>T, c.280T>A, c.924A>C and c.511G>A, resulting in a classic FD phenotype were identified. Moreover, FD was definitely diagnosed in five patients carrying the D313Y mutation. Eight D313Y carriers were presenting signs of FD despite not fulfilling the criteria of the disease, two had no FD signs and two others were apparently healthy.

Conclusions Four novel GLA pathogenic mutations are reported and evidence of pathogenicity of the D313Y mutation is provided. It seems that the D313Y mutation is related to a later-onset milder phenotype than the typical phenotype with normal lysoGb3 concentration. Our study underlines the significance of family member genotyping and newborn screening to avoid misdiagnoses and crucial delays in diagnosis and treatment of the disease.

  • fabry disease
  • D313y gla mutation
  • novel gla mutations
  • kidney biopsy
  • misdiagnosis

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

https://doi.org/10.1136/bmjopen-2017-017098

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    Strengths and limitations of this study

    • This is the largest series in the literature of clinically evaluated male and female carriers of the α-gal A gene (GLA) D313Y mutation supporting its possible pathogenicity that occasionally has been proved by renal biopsy.

    • Novel GLA mutations resulting in a classic Fabry disease phenotype are presented.

    • The main limitation is the lack of detailed clinical data in older participants.

    • Biopsies of affected organs, the gold standard of definite diagnosis, are not available in all cases.

    Introduction

    FD or Anderson-Fabry disease is an X-linked inherited metabolic disorder that results from mutations in the α-gal A gene (GLA gene), leading to reduction of the enzyme activity and subsequent accumulation of Gb3 (or GL-3) in plasma, urine and cellular lysosomes throughout the body. These depositions cause a multisystemic pathology with life-threatening manifestations, including renal failure, cardiac and cerebrovascular disease.1 2

    More than 900 currently known GLA mutations have been identified3 4 as causing a variety of clinical manifestations. Most of them are unique to a family (private) and therefore genotype–phenotype correlation is limited.5 Diagnosing FD is challenging due to the range of disorders that mimic the disease and the great variety of atypical clinical presentations. As a result, underdiagnosis and misdiagnosis of FD lead to late diagnosis, delays in appropriate treatment and a subsequent negative prognosis.6 Human genetic analysis must be performed to exclude or verify a GLA mutation.7 Once a diagnosis has been made, biochemical and molecular genetic analysis, as well as genetic counselling, should be made available to all family members.8 A detailed pedigree analysis for each patient presenting with FD is crucial,9 as it can inform the diagnosis of the proband and the identification of all at-risk relatives.10

    Our aim is to report four novel GLA mutations resulting in FD and provide evidence of pathogenicity of the D313Y mutation regarding which contradictory data have been presented in the literature.

    Methods

    Study design and setting

    This is a polycentric population screening study of individuals from Greece either demonstrating phenotypic traits suggestive of FD or belonging to families of patients with a definite FD diagnosis and fulfilling any one of the following inclusion criteria:

    • Definite diagnosis of FD.

    • Nephrological, cardiac or neurological symptoms suspicious of FD.

    • Relatives of patients with definite FD diagnosis.

    A cohort of 62 subjects from 19 unrelated families were involved in the study. Twenty-five were relatives of 9 patients with definite FD diagnosis and 18 were relatives of 10 individuals recruited as carriers of FD traits in whom a GLA mutation was detected. The presence of the D313Y mutation in a Greek population was examined by genotyping of 145 apparently healthy subjects (70 men, 75 women). Written informed consent was obtained from each subject or an accompanying relative if legally appropriate. The study was approved by the institutional review board of the University of Thessaly, Larissa.

    Clinical assessment

    Patients’ medical records were evaluated and a detailed medical history of the family members was obtained, especially regarding heart or kidney disease, cerebrovascular events, death at young age and respective causes of death. All study participants underwent a physical examination particularly focused on cardiac, renal and neurological signs and symptoms. A detailed pedigree was constructed for every family and newborn screening was performed.

    Laboratory evaluation

    In DBS, we measured α-Gal A activity in all male subjects using tandem mass spectrometry,11 lyso-Gb3 in all subjects using high-performance liquid chromatography and tandem spectrometry,12 as well as plasma and urine Gb3 concentration in selected cases using tandem mass spectrometry.13

    Optical and electron microscopy was occasionally performed for the study of kidney biopsies.

    Genotyping

    Genomic DNA was extracted from peripheral blood using the iPrep Pure Link DNA blood kit (Invitrogen, Thermofisher, USA) according to the manufacturer’s instructions. All coding regions and exon–intron splice junctions of the GLA gene were analysed in a targeted custom next-generation sequencing (NGS) platform (Ampliseq custom panel, Thermo Scientific). Analysis of primary data was conducted with Ion Reporter software v.5.2 (Thermo Scientific). Common polymorphisms (UCSC Common SNPs) were excluded and pathogenicity of variations was predicted by bioinformatic analysis using PhyloP, SIFT, Grantham and PolyPhen tools, in comparison to their global (1000 Genomes Global Minor Allele Frequency, ExAC) and European frequency (5000 Exomes European Minor Allele Frequency). The characterisation of variants was based on the recommendations of the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology.14

    Novel variants were verified by PCR in combination with Sanger sequencing. Amplification of GLA exons (including exon–intron boundaries) was performed in five reactions corresponding to exons 1, 2, 3, 4, and 5–7, using the primers included in the supplementary material. A total of 100–200 ng of genomic DNA was amplified by PCR in a 30 µL reaction mixture using 200 µM of each deoxynucleoside triphosphate, 30 pmol of each primer, 1.5 mM MgCl2 and 1.0 U Taq polymerase (Invitrogen, Thermofisher, USA) in a 10x buffer supplied by the manufacturer. Reaction conditions were as follows: for exons 1–3: 94ºC for 2 min, followed by 30 cycles of 30 s at 94ºC, 30 s at 58ºC, 30 s at 72ºC, and a final extension at 72ºC for 5 min. For exons 4 and 5–7: 94ºC for 2 min, followed by 32 cycles of 30 s at 94ºC, 30 s at 54ºC, 30 s for exon 4 or 75 s for exons 5–7 at 72ºC, and a final extension at 72ºC for 5 min. All PCR reactions were carried out in the Veriti 96-Well Thermal Cycler (Applied Biosystems, Thermofisher, USA). PCR engine apparatus and the emerging PCR products were purified using the PureLink PCR Purification Kit system (ThermoFisher Scientific, USA). Sequencing was performed using the primers described in the supplementary table, using a 3730 DNA Analyzer (Applied Biosystems, Thermofisher, USA) and BigDye Terminator DNA sequencing kit (Applied Biosystems, Thermofisher, USA), according to manufacturer’s instructions.

    Supplementary Material

    Supplementary material 1

    Results

    Nine (all with definite FD) out of the 62 genotyped subjects were carrying five previously described GLA mutations: c.334C>T (p.Arg112Cys, R112C), c.644A>G (p.Asn215Ser, N215S), c.1153A>C (p.Thr385Pro, T385P), c.453C>G (p.Tyr151Ter, Y151X) and c.782G>T (p.Gly261Val, G261V).

    The c.937G>T (p.Asp313Tyr, D313Y, NM_000169.2) mutation was revealed in 17 individuals (54±14, range 27–78 years), 7 men (61±11, range 45–78 years) and 10 women (49±15, range 27–70 years) but in none of the healthy subjects. Patients’ clinical and laboratory findings are presented in table 1. All male patients (61±11, range 45–78 years) presented with an α-gal A activity decreased in a range of 56.2–87.5% compared with normal, with the exception of one patient in whom α-gal A activity was within the normal range. LysoGb3 concentration was found normal (range 0.8–1.7 ng/mL) in all patients, while plasma and urine Gb3 concentration varied, as shown in table 1.

    View this table:
    Table 1

    Characteristics of patients carrying the D313Y mutation. Plasma and urine Gb3 concentration was measured only in patients 1, 4 and 5

    The diagnosis of FD was definitely posed according to the recently published criteria of the disease15 in five carriers of this mutation (54±9, range 45–65 years). The first (patient no. 1, table 1), a 52-year-old man, was initially diagnosed at the age of 48 with chronic kidney disease (CKD) stage III and was not presenting cardiac or other FD signs. Kidney biopsy performed because of non-nephrotic proteinuria, microscopic haematuria and raised serum creatinine, revealed focal and segmental glomerulosclerosis (FSGS) – collapsing variant. At that time, enzyme activity and plasma lyso-Gb3 concentration were normal. Three years after the initial presentation the patient had end-stage renal disease and extreme acroparesthesias. Evaluation of the kidney biopsy using a higher magnification uncovered focal cytoplasmic microvacuolisation of enlarged podocytes (figure 1), with α-gal A activity decreased by 50% and increased plasma (7.52 nmol/mL, reference: 0.8–4.52) and urine Gb3 concentration (147.49 nmol/g, reference: <29.00). The patient commenced dialysis and enzyme replacement therapy (ERT) with rapid clinical improvement.

    Figure 1
    Figure 1

    Optical microscopy findings of renal biopsy from a male patient with Fabry disease (FD) carrying the D313Y mutation of the GLA. (A) Glomerulus with segmental sclerosis – PAS ×400. (B) Segmental sclerosis with features of the ‘collapsing’ variant (arrow) – Jones’ silver ×400. (C) Pale appearing glomerulus with a small area of sclerosis adhering to Bowman’s capsule (arrow) – PAS ×400. (D) Cytoplasmic microvacuolisation of podocytes (arrow), suggestive of FD – PAS ×400.

    A second carrier of the D313Y mutation was a 46-year-old woman (patient no. 4, table 1) who had had a transient ischaemic attack and two ischaemic strokes that had been considered of unknown origin. On evaluation, 1 year after the last stroke, the patient appeared with microalbuminuria, oedema and acroparesthesias on both hands. The microalbuminuria was duplicated after 3 months and acroparesthesias worsened. Gb3 concentration was pathological in urine (54.08 nmol/g) but normal in plasma. LysoGb3 concentration was normal at that time and remained stable for one more year.

    The mother of the above patient (patient no. 5, table 1), 65 years old, had been diagnosed at the age of 50 with multiple sclerosis and was receiving relative medication, without clinical benefit. She was also receiving treatment for pain in the extremities that was attributed to rheumatoid arthritis. During recent years the patient had mobility impairment (reported as spastic quadriplegia after a neurological examination), depression and dementia. Evaluation of the patient revealed pathological plasma Gb3 concentration (4.7 nmol/mL), white matter lesion (WML) on brain MRI and normal kidney function. LysoGb3 concentration was normal and remained so during a 6-month follow-up.

    Another carrier of the D313Y mutation was a 45-year-old man (patient no. 7, table 1) on dialysis due to CKD by the age of 25. No kidney biopsy was performed at that time. He reported episodes of haematuria during childhood and adolescence, attributed at that time to vesicoureteral reflux. Enzyme activity was slightly decreased (2.4 μmol/L/hour, reference: ≥2.6) and plasma lyso-Gb3 concentration was normal. Brain MRI revealed WML and vertebrobasilar vessel changes. Moreover, the patient had increased echogenicity of the cardiac interventricular septum on the echocardiogram and sensorineural hearing loss of higher frequencies. The patient commenced ERT.

    The last patient with the D313Y mutation definitely diagnosed with FD was a 60-year-old woman (patient no. 17, table 1) who presented with cornea verticillata corneopathy, WML and ischaemic infarcts on brain MRI despite no stroke being reported, acroparesthesias and gastrointestinal (GI) symptoms (pain, diarrhoea) since adolescence, hypohidrosis, hearing loss and left ventricular hypertrophy (LVH).

    Among the remaining 12 D313Y mutation carriers there were two patients with no FD signs and eight patients (55±17, range 27–78 years) presenting with other FD signs, mainly neurological; however, they cannot document a definite diagnosis of FD. Especially patient no. 6, table 1 (62-year-old woman) had acroparesthesias and GI symptoms since adolescence and presented with lysoGb3 at 1.7 ng/mL (reference: ≥1.8). Accordingly, patient no. 16, table 1 (64-year-old man) presented with CKD, diabetes mellitus and hearing loss, while brain MRI showed multiple ischaemic infarcts despite no stroke being reported. The remaining two D313Y mutation carriers were apparently healthy.

    Novel GLA mutations (4) (figure 2) were detected in 13 members (39±18, range 1–69 years) of four unrelated families (table 2), all fulfilling the diagnostic criteria of a definite diagnosis of FD [15]. The c.835C>T mutation (p.Gln279Ter, Q279X) in exon 6 of the GLA gene was identified in four members (30±24, range 1–60 years) of a Greek family. The proband, a 31-year-old man, presented at the age of 23 with proteinuria (3.5 g/24 hours), microscopic haematuria, slightly deteriorated kidney function, right bundle brunch block, mild hypertension and angiokeratomas in the arms and the loin area. He reported pain in the extremities, especially during infections, and inability to sweat. The α-gal A activity was close to zero. Cardiac MRI showed moderate LVH. The kidney biopsy showed cytoplasmic vacuolization and extended lysosomal accumulations in all types of kidney cells, especially in the podocytes (figure 3). The patient is currently under ERT with beneficial results in regard with kidney function, proteinuria and pain. Three other members of the family were revealed having with the same mutation and all presented clinical signs of FD. The proband’s mother (60 years old) reported a possible TIA at the age of 32. Kidney examination showed albuminuria (>500 mg/24 hours), microscopic haematuria and normal kidney function. Cardiac MRI revealed severe LVH (cardiac interventricular septum over 19 mm) and on skin examination she showed angiokeratomas in the arms. Her mother (the proband’s grandmother) had died at the age of 62, due to cardiac arrest. She had severe LVH and acroparesthesias, which at that time were attributed to Raynaud’s phenomenon. The proband’s sister (27 years old) had elevated lyso-Gb3 concentration (2.7 ng/mL) and screening of her newborn daughter revealed the mutation too.

    Figure 2
    Figure 2

    Sanger confirmation of novel mutations.

    Figure 3
    Figure 3

    Electron microscopy findings of renal biopsy from a male patient with Fabry disease (FD) carrying the Q279X mutation. Multi-lamellated myelin figures (‘zebra’ bodies), a typical finding of FD, are marked with black arrows in (A) methylene blue semithin section, (B) tubular cells and a fibroblast and (C,D) podocytes.

    View this table:
    Table 2

    Clinical characteristics of patients with the four novel mutations

    Four patients (46±11, range 30–56 years) belonging to another Greek family were carrying the c.280T>A (p.Cys94Ser, C94S) mutation. The proband, a 48-year-old woman, was diagnosed with FD a year before after presenting with increased lyso-Gb3 concentration (5.4 ng/mL), increased plasma Gb3 concentration (6.14 nmol/mL), microalbuminuria of no other origin, cornea verticillata corneopathy, acroparesthesias in both hands and dyshidrosis. Clinical and laboratory data of the other affected members of the family are presented in table 2.

    The c.924A>C mutation (K308N – p.Lys308Asn) in exon 6 of the GLA gene was identified in three members of a Greek family (44±26, range 17–69 years). The proband, a 46-year-old man, presented at the age of 34 with albuminuria (0.5–0.6 g/24 hours), had microscopic haematuria for 10 years and slight hypertension. The kidney function was normal. Kidney biopsy showed slight mesangial proliferative damage and cytoplasmic microvacuolisation of podocytes. The α-gal A activity was almost zero. After a 10-year follow-up he had LVH and proteinuria (1.8 g/24 hours). The patient is currently under ERT. His mother and daughter carry the same mutation. The probands grandmother had died at the age of 68, with severe LVH and end-stage heart failure.

    Lastly, the c.511G>A mutation (G171S – p.Gly171Ser) in exon 3 of the GLA gene was identified in two members (37±4, range 34–39 years) of an Albanian family living in Greece. The proband, a 39-year-old man, was diagnosed at the age of 32 with severely deteriorated kidney function and proteinuria. No biopsy was performed at that time due to the small size of the kidneys. After nearly a year he presented with severe clinical and laboratory findings of acute renal failure and needed dialysis. Normal kidney function was never restored. FD was definitely diagnosed at the age of 37, as the α-gal A activity was extremely low and lyso-Gb3 concentration was 11.9 ng/mL. The patient had LVH, increased pulmonary artery diameter, dilatation of the ascending aorta and aortic valve stenosis, due to which he underwent a valve replacement surgery. Ophthalmological evaluation indicated lipid deposition with blurriness of the cornea. The patient is currently under ERT. His 34-year-old brother was identified with the same mutation and has extremely low α-gal A activity, lyso-Gb3 concentration 12,9 ng/mL and albuminuria of no other aetiology.

    Discussion

    The D313Y mutation

    Contradicting results about the pathogenicity of this mutation have been reported in the literature since its first description in 1993.16 The mutation has been detected in many series of patients presenting signs of FD.17–24 However, Niemann et al 25 describes this variant as non-pathogenic, although his two patients were presenting with decreased α-gal A activity. Similarly, Oder et al 26 support that the D313Y genotype does not lead to severe organ manifestations as seen in genotypes known to be causal for classical FD and Froissart et al 27 characterise the mutation as a ‘pseudodeficient allele’, implying that it is a sequence variant which encodes an enzyme that is transported to the lysosomes, where it has about 75% of normal enzymatic activity. The D313Y mutation has also been referred to as polymorphism,19 despite the fact that, according to the ExAC and 1000 Genomes databases, its frequency in the World and European population is below 1%. Finally, it must be mentioned that bioinformatics analysis shows that this mutation is predicted as probably damaging (PolyPhen-2) or damaging (SIFT).

    In our study, 5 of 17 carriers of the D313Y mutation (54±9, range 45–65 years) proved to have definite FD according to the recently published criteria of the disease.15 The presentation of the disease in our patients indicates that the mutation results in a milder phenotype, with later onset of symptoms. This phenotype, also including milder mono- or oligosymptomatic cases,19 is characterised as atypical or type 2.28 The late onset of clinical symptoms and the milder than the typical FD phenotype in these patients can be partly explained by the high α-gal A residual activity, since there is evidence that the mutated α-gal A reaches the lysosomes intracellularly.29 Actually, in all but one male D313Y carrier of our study, α-gal A activity was decreased. Another reason for the decreased activity of the D313Y enzyme in plasma could be a functional intolerance to blood plasma neutral pH conditions. This effect is irreversible and, once in contact with a neutral or basic pH environment, the D313Y enzyme remains inactive, even if transferred to optimal pH.21 29

    Interestingly, the vast majority of our patients with D313Y presented with neurological symptoms and signs. Moreover, one of them was misdiagnosed with MS while two carriers of the mutation, in whom a definite FD diagnosis had not been established yet, were diagnosed with MS and treated accordingly. Similarly the detailed study of the renal biopsy in one of our cases underlies the significance of early detection of Fabry-specific findings in cases with FSGS.

    Novel mutations

    The pathogenicity of the above-mentioned novel mutations has been undoubtfedly proved as all carriers had definite FD. Of these carriers, the c.835C>T (p.Gln279Ter, Q279X) is a nonsense mutation causing an interruption of the reading frame by a premature stop codon, which results in a truncated protein. A truncated protein and the subsequent loss of its functionality is strong evidence that the mutation is probably pathogenic for FD [14]. No amino acid change at this position has ever been described in the NCBI and Fabry Database (http://fabry-database.org/).30

    As far as the c.280T>A (C94S), c.924A>C (K308N), c.511G>A (G171S) mutations are concerned, bioinformatics analysis supports their disease-causing effect as they are predicted as probably damaging (PolyPhen-2) and/or damaging (SIFT). Further evidence of their pathogenicity could be the fact that the same aminoacid changes at the corresponding positions but in different nucleotides have already been described as disease causing.31–33

    Conclusions

    We report four novel GLA mutations causing FD. Moreover, we offer strong evidence that the D313Y mutation could be pathogenic. It seems that this mutation is related to a later-onset milder phenotype than the typical phenotype with normal lysoGb3.

    Additionally our study underlines the significance of family member genotyping, newborn screening and genetic counselling in avoiding misdiagnoses and crucial delays in diagnosis and treatment of the disease. Finally, we confirm the fact that heterozygous women may develop mild to severe FD and that the genotype–phenotype correlation does not exist even among members of the same families.

    Acknowledgments

    We appreciate the help and advice from A Andrikos, S Kouzouka, A Triantafillou, D Kaltsidou, A Kaliantzoglou, A Lysitska, K Papadopoulos, K Zoganas, G Tsivgoulis, Z Tegou, A Fountoglou, T Karapanagiotidis, S Patsialas.

    References

    1. 1.↵
      2. Germain DP
      . Fabry disease. Orphanet J Rare Dis 2010;5:30.doi:10.1186/1750-1172-5-30
      OpenUrlCrossRefPubMed
    2. 2.↵
      2. Schiffmann R
      . Fabry disease. Pharmacol Ther 2009;122:65–77.doi:10.1016/j.pharmthera.2009.01.003
      OpenUrlCrossRefPubMedWeb of Science
    3. 3.↵
      2. Abecasis GR ,
      3. Auton A ,
      4. Brooks LD , et al.
      An integrated map of genetic variation from 1,092 human genomes. Nature 2012;491:56–65.doi:10.1038/nature11632
      OpenUrlCrossRefPubMedWeb of Science
    4. 4.↵
      The Human Gene Mutation Database at the Institute of Medical Genetics in Cardiff. http://www.hgmd.cf.ac.uk/ (accessed 13 June 2017).
    5. 5.↵
      2. Laney DA ,
      3. Fernhoff PM
      . Diagnosis of Fabry disease via analysis of family history. J Genet Couns 2008;17:79–83.doi:10.1007/s10897-007-9128-x
      OpenUrlCrossRefPubMed
    6. 6.↵
      2. Mehta A ,
      3. Ricci R ,
      4. Widmer U , et al
      . Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey. Eur J Clin Invest 2004;34:236–42.doi:10.1111/j.1365-2362.2004.01309.x
      OpenUrlCrossRefPubMedWeb of Science
    7. 7.↵
      2. Gal A ,
      3. Hughes DA ,
      4. Winchester B
      . Toward a consensus in the laboratory diagnostics of Fabry disease - recommendations of a European expert group. J Inherit Metab Dis 2011;34:509–14.doi:10.1007/s10545-010-9261-9
      OpenUrlCrossRefPubMed
    8. 8.↵
      2. Winchester B ,
      3. Young E
      . Biochemical and genetic diagnosis of Fabry disease Chapter 18. In: Mehta A , Beck M , Sunder-Plassmann G , eds. Fabry disease: perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis, 2006.
    9. 9.↵
      2. Hughes DA ,
      3. Evans S ,
      4. Milligan A , et al
      ; A multidisciplinary approach to the care of patients with Fabry disease Chapter 35. In: Mehta A , Beck M , Sunder-Plassmann G , eds. Fabry disease: Perspectives from 5 years of FOS. Oxford: Oxford PharmaGenesis, 2006.
    10. 10.↵
      2. Laney DA ,
      3. Fernhoff PM
      . Diagnosis of Fabry disease via analysis of family history. J Genet Couns 2008;17:79–83.doi:10.1007/s10897-007-9128-x
      OpenUrlCrossRefPubMed
    11. 11.↵
      2. Chamoles NA ,
      3. Blanco M ,
      4. Gaggioli D
      . Fabry disease: enzymatic diagnosis in dried blood spots on filter paper. Clin Chim Acta 2001;308:195–6.doi:10.1016/S0009-8981(01)00478-8
      OpenUrlCrossRefPubMedWeb of Science
    12. 12.↵
      2. Aerts JM ,
      3. Groener JE ,
      4. Kuiper S , et al
      . Elevated globotriaosylsphingosine is a hallmark of Fabry disease. Proc Natl Acad Sci U S A 2008;105:2812–7.doi:10.1073/pnas.0712309105
      OpenUrlAbstract/FREE Full Text
    13. 13.↵
      2. Boscaro F ,
      3. Pieraccini G ,
      4. la Marca G , et al
      . Rapid quantitation of globotriaosylceramide in human plasma and urine: a potential application for monitoring enzyme replacement therapy in Anderson-Fabry disease. Rapid Commun Mass Spectrom 2002;16:1507–14.doi:10.1002/rcm.728
      OpenUrlCrossRefPubMedWeb of Science
    14. 14.↵
      2. Richards S ,
      3. Aziz N ,
      4. Bale S , et al
      . Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015;17:405–23.doi:10.1038/gim.2015.30
      OpenUrlCrossRefPubMed
    15. 15.↵
      2. Biegstraaten M ,
      3. Arngrímsson R ,
      4. Barbey F , et al
      . Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document. Orphanet J Rare Dis 2015;10:36.doi:10.1186/s13023-015-0253-6
      OpenUrlCrossRefPubMed
    16. 16.↵
      2. Eng CM ,
      3. Resnick-Silverman LA ,
      4. Niehaus DJ , et al
      . Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease. Am J Hum Genet 1993;53:1186–97.
      OpenUrlPubMedWeb of Science
    17. 17.↵
      2. Gaspar P ,
      3. Herrera J ,
      4. Rodrigues D , et al
      . Frequency of Fabry disease in male and female haemodialysis patients in Spain. BMC Med Genet 2010;11:19.doi:10.1186/1471-2350-11-19
      OpenUrlCrossRefPubMed
    18. 18.↵
      2. Wang RY ,
      3. Bodamer OA ,
      4. Watson MS , et al
      . ACMG Work Group on Diagnostic Confirmation of Lysosomal Storage Diseases. Lysosomal storage diseases: diagnostic confirmation and management of presymptomatic individuals. Genet Med 2011;13:457–84.
      OpenUrlCrossRefPubMed
    19. 19.↵
      2. Lukas J ,
      3. Giese AK ,
      4. Markoff A , et al
      . Functional characterisation of alpha-galactosidase a mutations as a basis for a new classification system in fabry disease. PLoS Genet 2013;9:e1003632.doi:10.1371/journal.pgen.1003632
      OpenUrlCrossRefPubMed
    20. 20.↵
      2. Böttcher T ,
      3. Rolfs A ,
      4. Tanislav C , et al
      . Fabry disease - underestimated in the differential diagnosis of multiple sclerosis? PLoS One 2013;8:e71894.doi:10.1371/journal.pone.0071894
    21. 21.↵
      2. Lenders M ,
      3. Duning T ,
      4. Schelleckes M , et al
      . Multifocal white matter lesions associated with the D313Y mutation of the α-galactosidase A gene. PLoS One 2013;8:e55565.doi:10.1371/journal.pone.0055565
    22. 22.↵
      2. Samuelsson K ,
      3. Kostulas K ,
      4. Vrethem M , et al
      . Idiopathic small fiber neuropathy: phenotype, etiologies, and the search for fabry disease. J Clin Neurol 2014;10:108–18.doi:10.3988/jcn.2014.10.2.108
      OpenUrl
    23. 23.↵
      2. Becker J ,
      3. Rolfs A ,
      4. Karabul N , et al
      . D313Y mutation in the differential diagnosis of white matter lesions: Experiences from a multiple sclerosis outpatient clinic. Mult Scler 2016;22:1502–5.doi:10.1177/1352458516638747
      OpenUrlCrossRefPubMed
    24. 24.↵
      2. De Brabander I ,
      3. Yperzeele L ,
      4. Ceuterick-De Groote C , et al
      . Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young. Clin Neurol Neurosurg 2013;115:1088–93.doi:10.1016/j.clineuro.2012.11.003
      OpenUrlCrossRefPubMed
    25. 25.↵
      2. Niemann M ,
      3. Rolfs A ,
      4. Giese A , et al
      . Lyso-Gb3 indicates that the Alpha-Galactosidase A mutation D313Y is not clinically relevant for Fabry Disease. JIMD Rep 2013;7:99–102.doi:10.1007/8904_2012_154
      OpenUrl
    26. 26.↵
      2. Oder D ,
      3. Üçeyler N ,
      4. Liu D , et al
      . Organ manifestations and long-term outcome of Fabry disease in patients with the GLA haplotype D313Y. BMJ Open 2016;6:e010422.doi:10.1136/bmjopen-2015-010422
    27. 27.↵
      2. Froissart R ,
      3. Guffon N ,
      4. Vanier MT , et al
      . Fabry disease: D313Y is an alpha-galactosidase A sequence variant that causes pseudodeficient activity in plasma. Mol Genet Metab 2003;80:307–14.doi:10.1016/S1096-7192(03)00136-7
      OpenUrlCrossRefPubMedWeb of Science
    28. 28.↵
      2. Lenders M ,
      3. Weidemann F ,
      4. Kurschat C , et al
      . Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variant. Orphanet J Rare Dis 2016;11:54.doi:10.1186/s13023-016-0441-z
      OpenUrl
    29. 29.↵
      2. Yasuda M ,
      3. Shabbeer J ,
      4. Benson SD , et al
      . Fabry disease: characterization of alpha-galactosidase A double mutations and the D313Y plasma enzyme pseudodeficiency allele. Hum Mutat 2003;22:486–92.doi:10.1002/humu.10275
      OpenUrlCrossRefPubMedWeb of Science
    30. 30.↵
      Meiji Pharmaceutical university. http://fabry-database.org (accessed 15 Feb 2017).
    31. 31.↵
      2. Shabbeer J ,
      3. Yasuda M ,
      4. Benson SD , et al
      . Fabry disease: identification of 50 novel alpha-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutations. Hum Genomics 2006;2:297–309.doi:10.1186/1479-7364-2-5-297
      OpenUrlCrossRefPubMed
    32. 32.↵
      2. Blaydon D ,
      3. Hill J ,
      4. Winchester B
      . Fabry disease: 20 novel GLA mutations in 35 families. Hum Mutat 2001;18:459.doi:10.1002/humu.1219
      OpenUrlPubMed
    33. 33.↵
      2. Shimotori M ,
      3. Maruyama H ,
      4. Nakamura G , et al
      . Novel mutations of the GLA gene in Japanese patients with Fabry disease and their functional characterization by active site specific chaperone. Hum Mutat 2008;29:331.doi:10.1002/humu.9520
      OpenUrlPubMed

    Footnotes

    • Contributors KK: collection, analysis and interpretation of the data, pedigree analysis, literature review, drafting and revision of the manuscript. KS: renal biopsy and analysis on electron microscope. PP: renal biopsy and analysis on optical microscope. MS, MZ and GL: genotyping and bioinformatics analysis. KS, PP, EM, PK, CK, AO, JK: treating physicians of patients. AEG: design and coordination of the study, revision of the manuscript. All authors approved the final version of the manuscript.

    • Funding The study has been partially supported by a grant from the Research Committee of the University of Thessaly.

    • Competing interests KK received travel assistance from Shire and Genzyme and speaker’s honoraria from Shire. KS received travel assistance and speaker’s honoraria from Shire. PP and AO received travel assistance from Genzyme and Shire. CK received travel assistance from Shire. AEG received research grants from Shire. The authors MZ, GL, MS, EM, PK, JK, report no competing interests.

    • Ethics approval This report was approved by the institutional review board of the University of Thessaly, Larissa. Written informed consents for participation were obtained from patients.

    • Provenance and peer review Not commissioned; externally peer reviewed.

    • Data sharing statement All data supporting our findings are included in the manuscript.

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