Affiliation:
1. Shaheed Suhrawardy Medical College Hospital Dhaka Bangladesh
2. Bangladesh College of Physicians and Surgeons Dhaka Bangladesh
Abstract
Key Clinical MessageBardet–Biedl syndrome (BBS) is a rare autosomal recessive ciliopathic disorder. Because of its low prevalence and wide spectrum of clinical features, many patients remain undiagnosed. We report a case of a 14‐year‐old boy with a typical phenotype of BBS who remains undiagnosed until the development of end‐stage renal disease.
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