exome sequencing identifies a novel sgca gene mutation in an iranian family with limb girdle muscular dystrophy: a case report

Introduction: autosomal recessive limb-girdle muscular dystrophy (lgmd) is a rare congenital muscular dystrophy type. this inherited disease is one of the most common diseases resulting in severe physical health problems for infants. genetic studies have shown that several gene mutations cause limb-girdle muscular dystrophy. this study aimed to report the case of a 10-year-old boy from an iranian consanguineous family diagnosed with congenital muscular dystrophy and a causative genetic abnormality. case presentation: in this report, whole exome sequencing (wes) followed by sanger sequencing was performed to diagnose the possible genetic defects in patients with lgmd. a novel homozygous disease-causing sgcagene mutation (p.a107fs:c.319-329del) was found in exon 10 (nm_000023.4). both parents were heterozygous for the detected mutation. conclusions: it was concluded that the identified sgcagene mutation was a pathogenic variant causing autosomal recessive lgmd.