Identification of Genetic Variants Causing Paediatric Cataract in Myanmar.

Journal: Clinical Genetics
Published:
Abstract

Genetic testing for paediatric cataract detects a cause in 50%-70% of affected children but is as low as 20% in some reports. We screened 180 cataract-related genes in 22 children (from 20 families) with paediatric cataract from Myanmar using whole-exome sequencing. Pathogenic or likely pathogenic variants were identified in 45% (9/20) of probands in genes MIP, COL2A1, NHS, GJA8, GJA3, CRYGC, CRYBB2, PAX6 and SLC7A8. Variants of uncertain significance likely to be important were identified in three children for a maximum diagnostic rate of 12/20 probands (60%) comparable to other reports. This is the first study to examine the genetics of paediatric cataract in Myanmar.

Authors
Johanna Jones, Daisy Boardman, Khine Nweni, Franoli Edo, Isabelly Barros De Lima, Pakdhipat Lertsinpakdee, Soe Hlaing, Robert Casson, Ashwin Mallipatna, Ye Win, Bennet Mccomish, Naing Lin, James Muecke, Andy Griffiths, Martin Holmes, Than Aung, Kathryn Burdon
Relevant Conditions

Cataract, Congenital Cataract