11p13 deletion

WAGR syndrome is a rare genetic disorder associated with the deletion of chromosome 11p13, involving genes WT1 and PAX6, and features Wilms’ tumor, aniridia, genitourinary anomalies, as well as varying degrees of intellectual disabilities. Some other findings may include obesity, glaucoma, cataracts, kidney failure, congenital diaphragmatic hernia, and autism. Wang... Read More