Cytology and Genetics, volume 58, issue 5, pages 486-492

Targeted Sequencing of HEXA Gene Shows Missense Substitution (p.Arg499His) in a Large Pakistani Family with Tay-Sachs Disease

Fariya Khan Bazai 1
Mehmood Ul Hassan 1
Hani Tayyab 2
Sara Naudhani 3
Sami Siraj 4
Muhammad Tariq 5
Sajjad Ali Shah 6
Jamil Ahmad 7
Shakeela Daud 3
Show full list: 9 authors
1
 
Quetta Institute of Medical Sciences, Quetta, Pakistan
2
 
Department of Biochemistry and Biomedical Sciences, Macmaster University, Ontario, Canada
5
 
Division of Science and Technology, University of Education, Lahore, Pakistan
6
 
Institute of Biotechnology and Microbiology, Bacha Khan University, Charsadda, Pakistan
Publication typeJournal Article
Publication date2024-09-20
scimago Q4
SJR0.174
CiteScore1.1
Impact factor0.5
ISSN00954527, 19349440
Abstract
Tay-Sachs disease or GM2 gangliosidosis, is caused by a deficiency of beta-hexosaminidase A (HEXA), resulting in lysosomal accumulation of GM2 ganglioside. However, deficiencies or reduced activities of HEXA and HEXB result in Sandhoff disease. The patients manifest with the macular cherry-red spots due to lipid-laden ganglion cells, hypotonia, low muscle tone, intractable seizures, developmental arrest, blindness, and neurological deterioration. The aim of this study was to identify the TSD-causing variant in a large Pakistani family showing typical symptoms of Tay-Sachs disease. Here, we studied a large Pakistani family with six TSD patients for the identification of the pathogenic variant by targeted DNA sequencing. As a result, we identified a missense substitution (p.Arg499His) in exon 13 of HEXA that was completely cosegregated among affected and normal individuals. In conclusion, we identified a missense substitution (p.Arg499His) in HEXA gene in a large consanguineous Pakistani family and further enriched the mutational spectrum of HEXA through Pakistani patients for the early diagnosis of the disease.
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