Founder mutation in KCNJ10 in Pakistani patients with EAST syndrome. Issue 5 (7th June 2016)

• Record Type: Journal Article
• Authors: Abdelhadi, Ola; Iancu, Daniela; Tekman, Mehmet; Stanescu, Horia; Bockenhauer, Detlef; Kleta, Robert
• Is Part Of: Molecular genetics & genomic medicine. Volume 4:Issue 5(2016)
• Page Start: 521
• Page End: 526
• Publication Date: 2016-06-07
• Subjects: Ataxia -- epilepsy -- kidney -- Kir4.1 -- potassium channel -- tubulopathy; Medical genetics -- Periodicals; Genomics -- Periodicals; 616.042
• DOI: 10.1002/mgg3.227
• Languages: English
• ISSNs: 2324-9269

Abstract

Abstract: Background: EAST syndrome is an autosomal recessive disorder caused by loss‐of‐function mutations in the gene KCNJ10 . Among the 14 pathogenic mutations described so far, the p.R65P mutation stands out as the most frequent one and is particularly associated with patients of Pakistani origin. As a result we aimed to establish the existence of a potential founder effect in the Pakistani population. Methods: To this end, we genotyped 12 patients from seven families and we compared disease haplotypes with ethnically matched control chromosomes. This haplotype was used together with demographic data for Pakistan to estimate the age of this founder mutation. Results: We identified a small homozygous 0.694 Mb region around the KCNJ10 p.R65P mutation that had identical haplotypes in all of the patients which were completely absent in the control sample. Based on current demographic data and knowledge about disease frequency, we estimate that this particular p.R65P mutation arose 20 generations (about 500 years) ago. Conclusion: By knowing the prevalent mutation in a given population more efficient diagnostics can be performed and the families can benefit from specific counseling. Abstract : Providing genetic evidence for a founder mutation in a rare kidney, brain, and inner ear disease in a Pakistani population.