ea0099ep1131 | Reproductive and Developmental Endocrinology | ECE2024
El Haddad Hemmet
, Abou Farha Manal
, Sameh Ihab
, Fayed Ahmed
, Ezzat Asma
, Salam Randa
, Abdalla Alaa
, Ihab Sara
, Essam Haader
, Khaled Rodina
Introduction: Bardet–Biedl syndrome is a rare autosomal recessive disorder with a wide range of clinical features. The primary clinical features include rod-cone dystrophy, postaxial polydactyly, central obesity, cognitive impairment, male hypogonadism and renal dysfunction.Case report: 22 Year old male, mentaly retarded with Bardet Biedle syndrome presented to our ER with vomiting and generalized weakness for 1 week. There was no history of fever, ...