Homozygous nonsense mutation in SGCA is a common cause of limb‐girdle muscular dystrophy in Assiut, Egypt. Issue 4 (24th August 2016)

• Record Type: Journal Article
• Authors: Reddy, Hemakumar M.; Hamed, Sherifa A.; Lek, Monkol; Mitsuhashi, Satomi; Estrella, Elicia; Jones, Michael D.; Mahoney, Lane J.; Duncan, Anna R.; Cho, Kyung‐ah; Macarthur, Daniel G.; Kunkel, Louis M.; Kang, Peter B.
• Is Part Of: Muscle & nerve. Volume 54:Issue 4(2016)
• Page Start: 690
• Page End: 695
• Publication Date: 2016-08-24
• Subjects: founder effect -- homozygosity mapping -- limb‐girdle muscular dystrophy -- sarcoglycanopathy -- whole exome sequencing; Neuromuscular diseases -- Periodicals; Muscles -- Periodicals; Nerves -- Periodicals; 616.74
• DOI: 10.1002/mus.25094
• Languages: English
• ISSNs: 0148-639X

Abstract

ABSTRACT: Introduction: The genetic causes of limb‐girdle muscular dystrophy (LGMD) have been studied in numerous countries, but such investigations have been limited in Egypt. Methods: A cohort of 30 families with suspected LGMD from Assiut, Egypt, was studied using immunohistochemistry, homozygosity mapping, Sanger sequencing, and whole exome sequencing. Results: Six families were confirmed to have pathogenic mutations, 4 in SGCA and 2 in DMD . Of these, 3 families harbored a single nonsense mutation in SGCA, suggesting that this may be a common mutation in Assiut, Egypt, originating from a founder effect. Conclusions: The Assiut region in Egypt appears to share at least several of the common LGMD genes found in other parts of the world. It is notable that 4 of the 6 mutations were ascertained by means of whole exome sequencing, even though it was the last approach adopted. This illustrates the power of this technique for identifying causative mutations for muscular dystrophies. Muscle Nerve 54 : 690–695, 2016