| Literature DB >> 34373539 |
Hessa Al-Kandari1,2, Dalia Al-Abdulrazzaq1,3, Lena Davidsson1, Rasheeba Nizam4, Sindhu Jacob4, Motasem Melhem4, Sumi Elsa John4, Fahd Al-Mulla5.
Abstract
Genetic variants responsible for Maturity-Onset-Diabetes of the Young (MODY) in Kuwait were investigated. A newly established a National Referral Clinic, the Dasman Diabetes Institute (DDI-NRC), assessed forty-five members from 31 suspected MODY families by whole exome sequencing. Thirty-three of the 45 samples were independently sequenced at the DDI-NRI, Exeter University, UK ( https://www.diabetesgenes.org/ ) using targeted 21-gene panel approach. Pathogenic mutations in GCK, HNF1A, HNF1B, HNF4A, and PDX1 confirmed MODY in 7 families, giving an overall positivity rate of 22.6% in this cohort. Novel variants were identified in three families in PDX1, HNF1B, and HNF1B. In this cohort, Multiplex Ligation-dependent Probe Amplification assay did not add any value to MODY variant detection rate in sequencing negative cases. In highly selected familial autoantibody negative diabetes, known MODY genes represent a minority and 77.3% of the familial cases have yet to have a causal variant described.Entities:
Year: 2021 PMID: 34373539 DOI: 10.1038/s41598-021-95552-z
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379