Bardet–Biedl syndrome: Delayed diagnosis in a 14‐year‐old child with end‐stage renal disease

Author:

Rasel Mohammad12ORCID,Istiak Ashif12ORCID,Saiara Afra12,Al‐Jubair Abdullah1,Matin Shariful1,Roy Gobinda Chandra1

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.

Publisher

Wiley

Subject

General Medicine

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