Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family

Infantile neuroaxonal dystrophy (INAD) is a rare hereditary neurological disorder caused by mutations in the PLA2G6 gene [1]. The disease commonly affects children below 3 years of age and presents with delay in motor skills, optic atrophy and progressive spastic tetraparesis. Brain MRI shows cerebellar atrophy, white matter abnormalities and hypointense globus pallidus. Infants with the disease are usually normal at birth but deteriorate rapidly and rarely live beyond their first decade [2].

The incidence and prevalence of INAD is currently unknown [3]. More than 85% of cases are caused by mutations in PLA2G6 gene, while the remainder has unknown genetic cause. The protein product of PLA2G6 gene has important roles in the metabolism of membrane phospholipids. Sequencing analysis of PLA2G6 gene has identified missense, nonsense, splicing disruption variants and insertion/deletions with genotype/phenotype correlation: loss of function mutations are usually associated with more severe forms of the disease, while compound heterozygous variants have usually milder presentation [4].

Two Sudanese siblings from a consanguineous family (F25) from White Nile area in central Sudan presented with delayed motor and intellectual development. Patient 1 presented at age 24 months with walking difficulty due to muscle weakness and poor speech. The patient was able to sit without support at age 6 months; she started walking with assistance at age 12 months but lost her ability to walk at age 2 years. She was able to say “dada, mama” at age 8 months but lost this ability by age 20 months. At age 2.5 years, the patient became non-ambulatory and completely lost her speech ability. Patient 2 presented with the same clinical features but started earlier at age 18 months, he was able to sit with support and say “dada, mama” at ages 6 and 8 months respectively. He was able to walk with support at age 12 months but at the time of examination, he was only able to roll in bed. Both patients had progressive dysphagia for both solids and liquids and behavioral changes (lack of communication in patient 1 and significant irritability in patient 2). On examination both patients had normal upper and lower limbs tone and hyperreflexia in all limbs with up-going plantar response. Cognitive status of the two patients was difficult assess but both patients appeared to be non-attentive. Both patients had marked left sided visual impairment and bilateral optic atrophy. There were no extrapyramidal signs. Brain MRI showed bilateral and symmetrical T2/FLAIR hyperintense signal changes in periventricular areas, basal ganglia, globus pallidus and to lesser degree head of caudate nucleus and putamen as well as the cerebellum. Mild generalized cerebellar atrophy was found in both patients but there was no evidence of brain iron accumulation (hypointense signals in T2 and hyperintense signals in T1 weighted images), Fig. 1.

INAD is a typical example of a rare hereditary neurological disease with high mortality and morbidity [2]. Mutations in PLA2G6 gene causing INAD have been described previously in many studies [4‐13]. These were more commonly homozygous missense variants or deletions which lead to loss of protein function. Splice site variants have been rarely reported although they are considered also loss of function mutations [14]. The spectrum of causative mutations is obscure and possibly unknown in patients from Sub Saharan Africa despite the well-known genetic heterogeneity in this region [15]. This is the first study of INAD in Sudan and it showed a novel homozygous splicing mutation (c.1427 + 2 T > C) in exon 10 of PLA2G6 gene of two siblings with typical clinical features. The variant segregated with the disease; both parents were heterozygous and all unaffected family members had either the wild type genotype or were heterozygous. Mutations in exon 10 have been previously reported in association with INAD in dogs [16]. This comports with its role in the pathogenesis of the disease in this family. The effect on mRNA could not be checked however as no cells were available from the patients.

According to the latest ACMG guidelines [17], this variant has one very strong (loss of function mutation) and three supporting evidence for its pathogenicity (segregation with the disease, multiple computational evidence and specific patients’ phenotype). In addition, this variant was absent in Exac and 1000 genome browser databases and has a total allele frequency of 0.4065 × 10^− 5 in genomAd browser with no reported homozygotes. Furthermore, the (c.1427 + 2 T > C) variant is highly predicted to cause skipping of exon 10 during mRNA maturation. Splicing alteration leads to skipping of an exon or retention of an intron both significantly altering protein structure and function [18]. Therefore this variant can be currently annotated as “pathogenic”.