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01.12.2012 | Case report | Ausgabe 1/2012 Open Access

Journal of Medical Case Reports 1/2012

Chromosomal 16p microdeletion in Rubinstein-Taybi syndrome detected by oligonucleotide-based array comparative genomic hybridization: a case report

Zeitschrift:
Journal of Medical Case Reports > Ausgabe 1/2012
Autoren:
Md A Mohd Fadley, Azli Ismail, Thong Meow Keong, Narazah Mohd Yusoff, Zubaidah Zakaria
Wichtige Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1752-1947-6-30) contains supplementary material, which is available to authorized users.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

MFMA conducted the array CGH work, performed the data analysis relevant to this case report and drafted this manuscript. TMK provided all clinical details and genetic counseling for the patient and her parents. AI performed the checking procedures for this case and reviewed the manuscript. TMK, NMY, ZZ reviewed the manuscript. All authors read and approved the final manuscript.

Introduction

Rubinstein-Taybi syndrome (RSTS) is a well delineated multiple congenital anomaly syndrome characterized by mental retardation, broad thumbs and toes, short stature and specific facial features [1]. The syndrome is, at least in part, caused by a microdeletion at chromosome 16 p13.3 or by mutations in the gene for the cyclic adenosine monophosphate-response element-binding protein (Crebbp), which is located at 16 p13.3 [2]. The occurrence is generally sporadic and birth prevalence is one in 100, 000 to 125, 000 [2]. About 55% of patients have cytogenetic or molecular abnormalities in the Crebbp or E1A binding protein p300 (Ep300) gene, leaving the diagnosis in 45% of patients to rest on clinical features only [3]. However, due to the absence of a distinct clinical presentation and the limitation of routine chromosomal analysis techniques, definitive diagnosis in younger children is difficult.
Conventional cytogenetic analysis of patients with syndromic features has largely reported findings of a normal karyotype. This necessitates the adoption of a more sensitive method to detect the occurrence of any submicroscopic chromosomal aberration. Microarray-based comparative genomic hybridization (array-CGH) is a high-throughput technique that offers rapid genome-wide analysis at high resolution. Array-CGH is designed to detect not only genome-wide chromosomal and segmental deoxyribonucleic acid (DNA) copy number changes, but also map and measure the regions of amplification, which may be associated with a wide range of diseases, from developmental disorders to cancer. The use of current array-CGH technology enables the detection of submicroscopic chromosomal aberrations at multiple loci and localization of disease gene regions for subsequent candidate gene identification.

Case presentation

Our patient was a three-year-old Malaysian Chinese girl. She was the second of two children. Her parents were healthy and non-consanguineous. There was no significant family history. She was delivered at term via an elective lower segment Cesarean section with a birth weight of 2.63 kg. A pelvic cyst was detected during the antenatal period, but this had resolved spontaneously when a repeat ultrasound was done at six weeks of age. She was noted to have inspiratory stridor and a diagnosis of laryngomalacia was made at 10 weeks of age. She showed a failure to thrive with slow feeding. Her growth parameters of weight, length and head circumference were below the third percentiles. She was given nasogastric feeding. A barium swallow showed no abnormalities. Her weight gradually improved when a percutaneous gastroenterostomy tube was inserted. A physical examination at one year of age showed inspiratory stridor and dysmorphic features, such as a prominent nasal bridge, hypertelorism, down-slanting palpebral fissures, a small mouth, micrognathia, low set ears, sparse hair and bilateral broad thumbs and great toes (Figure 1). There was a soft systolic murmur heard on auscultation of the left sternal edge. She had generalized hypotonia but no other neurological deficits. She had mild to moderate global developmental delay, was only able to scribble, climb steps slowly and hold on to the rails, had no meaningful word in her speech but was able to obey simple commands and communicate with sign language. Investigations showed that she had a normal full blood count and metabolic studies, a normal karyotype and normal results for a DNA methylation study for Prader-Willi syndrome. An echocardiogram showed a moderate size atrial septal defect. She had refractive errors and failed a distraction test. A peripheral blood sample was sent for array-CGH analysis at the age of one year and seven months.
Cytogenetic analyses of our patient and her healthy parents were performed by G-banding techniques at 550 bands of resolution on metaphase chromosomes obtained by standard procedures from peripheral blood lymphocytes. Molecular karyotyping was performed using commercially available high resolution 244K 60-mer oligonucleotide microarray slide (Human Genome CGH Microarray 244A Kit, Agilent Technologies, Santa Clara, CA, USA) according to the manufacturer's protocol. This platform allows a genome-wide survey and molecular profiling of genomic aberrations with an average resolution of about 10 kb.
Cytogenetic analysis of our patient and her parents showed that they had normal karyotypes. Array-CGH analysis revealed a microdeletion of chromosome 16 involving band p13.3, with the first clone locating at 3, 651, 083 base pairs on proximal 16 p13.3 and the last clone locating at 3, 771, 464 base pairs on distal 16 p13.3, according to the University of California Santa Cruz Genome Browser on Human March 2006 Assembly (NCBI36/hg18). The size of the deletion was estimated to be about 120 kb. The deletion was confirmed by a dye swap experiment of array-CGH. Multiplex ligation-dependent probe amplification (MLPA) experiments were performed to validate the array-CGH finding and to determine the parental origin of the deletion. The deletion was confirmed to be hemizygous and de novo using SALSA MLPA kit P313-A1 CREBBP (Microbiology Research Centre Holland, Amsterdam, The Netherlands).

Discussion

Chromosomal imbalances are known causes of genetic disorders and often result in a syndromic condition. We here describe a three-year-old girl with a global developmental delay, dysmorphic features and multiple congenital anomalies, carrying a 120 kb microdeletion of chromosome 16 p13.3 detected by array-CGH (Figure 2). The deletion region encompasses two known genes, for tumor necrosis factor receptor-associated protein 1 (Trap1) and Crebbp. It has been demonstrated that the Trap1 gene is located on chromosome 16 p13.3 between 3, 648, 039 and 3, 707, 599 base pairs while the Crebbp gene is located on chromosome 16 p13.3 between 3, 716, 570 and 3, 870, 712 base pairs (NCBI36/hg18). The deleted region in our patient, identified by array-CGH, was located between 3, 651, 083 and 3, 771, 464 base pairs. Crebbp was partially deleted while its neighbor gene, Trap1, was deleted. Further study by MLPA technique confirmed the deletion within the Crebbp gene to be de novo and hemizygous from exons 6 to 31, which corresponds to between 3, 717, 675 and 3, 772, 856 base pairs (Figure 3). This MLPA finding is consistent with the array-CGH result.
In most cases, cytogenetic rearrangements at chromosome 16 p13.3 or submicroscopic deletions within 16 p13 were found to be caused by heterozygous molecular mutations in Crebbp gene [4, 5]. The Crebbp gene has been reported to be associated with RSTS and is thought to be responsible for the core clinical manifestations of RSTS in our patient. Crebbp (OMIM: 600140) is a transcription coactivator and functions as a potent histone acetyltransferase, both of which are essential to normal development [6]. The Crebbp gene is involved in different signaling pathways and in certain cellular functions, such as DNA repair, cell growth, differentiation, apoptosis and tumor suppression. Crebbp gene deletion [7] or exon deletion [8] are demonstrated in about 8% to 12% of patients. EP300 (OMIM: 602700) mutations were also identified as another rare cause of RSTS in 3% of patients [6]. The Human Gene Mutation Database (http://​www.​hgmd.​org) holds, at present, 92 different mutations in the Crebbp gene - 13 missense substitutions, 20 nonsense substitutions, 10 splicing substitutions, 16 small deletions, nine small insertions, two small indels, 19 gross deletions, one gross insertion and two complex rearrangements. Previous studies of patients with RSTS indicated 16 p13.3 deletions of up to 560 kb to 650 kb and including the 5'- and 3'-flanking regions of the Crebbp gene [4, 8, 9]. Recently, intragenic deletions were detected in two RSTS patients using an exon coverage microarray platform; one in a male patient resulting from deletion of two exons within the Crebbp gene and the other in a female patient resulting from deletion of four exons within the Ep300 gene [10].
Trap1 (OMIM: 606237) is a mitochondrial 90-kilodalton heat shock protein (Hsp90). Hsp90 proteins are important and highly conserved molecular chaperones that have key roles in signal transduction, protein folding, protein degradation and morphologic evolution. Hsp90 proteins normally associate with other co-chaperones and play important roles in folding newly synthesized proteins or stabilizing and refolding denatured proteins after stress. The human Hsp90 family includes 17 genes that fall into four classes. Six genes, Hsp90AA1, Hsp90AA2, Hsp90N, Hsp90AB1, Hsp90B1 and Trap1, were recognized as functional, and the remaining 11 genes were considered putative pseudogenes [11]. Although Trap1 has not been associated with human disease, the importance of this gene warrants attention. In addition, a small subset of RSTS cases caused by 16 p13.3 microdeletions involving neighboring genes of Crebbp have recently been suggested to be a true contiguous gene syndrome called severe RSTS, or 16 p13.3 deletion syndrome (OMIM: 610543) [12]. Bartsch et al. [12] concluded that contiguous gene deletions up to 3 Mb, all of which included Crebbp, Trap1 and deoxyribonuclease 1 gene (DNase1), will result in severe RSTS. A case described by Wójcik et al. [13] showed an approximate 520.7 kb microdeletion on 16 p13.3, involving Crebbp, the Adenyl cyclase 9 and Sarcalumenin genes, in a two-year-old female with RSTS. Besides most of the typical features of RSTS, their patient had corpus callosum dysgenesis and a Chiari type I malformation which required neurosurgical decompression. These evidences demonstrated that microdeletion involving neighboring genes to Crebbp gene might be responsible for the additional features in RSTS. In addition, our finding merits further interest because no cases of microdeletion 16 p13.3 with contiguous gene deletion, comprising Crebbp and Trap1 genes, have been described in typical RSTS patients.
It is noteworthy that as our patient grew older her clinical features became increasingly more consistent with RSTS. Most of the typical RSTS features as described by Hennekam [3] were observed. These features include a prominent nasal bridge, down-slanting palpebral fissures, a small mouth, low set ears, bilateral broad thumbs and great toes and growth retardation. Congenital heart defects (mainly patent ductus arteriosus, ventricular septal defect and atrial septal defect) were observed in 32% of patients [3]. Although excessive hair growth (hirsutism) is found in 75% of cases [14], our patient interestingly had sparse hair, a condition that has not previously been reported in a typical RSTS patient. Whether this manifestation is affected by the abnormality of Trap1 is uncertain. Since our patient showed most of the typical features of RSTS, we hypothesized that this region is haplosufficient inasmuch that the deletion of Trap1 bore no significant complication to our patient. However, further studies are needed to clarify the potential role of Trap1 in 16 p13.3 microdeletion.
RSTS can be regarded as a microdeletion syndrome with a low rate of microdeletions, as only 4% to 25% of patients with RSTS were found to have the Crebbp deletion on chromosome 16 p13.3 when using fluorescence in situ hybridization [7]. It is critical that the diagnosis of an unexplained syndromic condition, especially in young patients, is confirmed by an advanced laboratory technique such as array-CGH. An accurate diagnosis will enable the precision of long-term care and a health surveillance program for patients with RSTS. This includes regular monitoring for the emergence of tumors, immunodeficiencies, early surgical correction of surgical and orthopedic complications, genetic counseling for future pregnancy and prenatal diagnosis. In addition, there is little published literature of longitudinal studies on this syndrome in the population. The finding from our patient adds to the increased awareness of RSTS variability in the population. Our case has been deposited into the Database of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources (DECIPHER-Patient ID: 254034) [15].

Conclusion

We found this case worthy of reporting as, to date, there is very little documented evidence of this syndrome ascertained by microarray analysis. Here, we demonstrate the superiority of the array-CGH technique over conventional techniques in the screening and detection of clinically significant genomic imbalances in the human genome. Array-CGH is a reliable and powerful tool in the investigation of rare genetic conditions, especially cases with a highly variable phenotype and variable aberrations such as Rubinstein-Taybi syndrome.

Consent

Written informed consent was obtained from the parents of our patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Acknowledgements

The authors thank the Director General of Health, Malaysia, for permission to publish this scientific paper. We would also like to thank Deputy Director General of Health (Research & Technical Support, Ministry of Health Malaysia) and the Director of the Institute for Medical Research for their support. We would also like to express our gratitude to Ten Sew Keoh for her help in language and writing assistance. This research was funded by the Ministry of Health Malaysia (JPP-IMR 07-041).
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

MFMA conducted the array CGH work, performed the data analysis relevant to this case report and drafted this manuscript. TMK provided all clinical details and genetic counseling for the patient and her parents. AI performed the checking procedures for this case and reviewed the manuscript. TMK, NMY, ZZ reviewed the manuscript. All authors read and approved the final manuscript.

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