hrp0097p1-134 | Multisystem Endocrine Disorders | ESPE2023
Gao Shiyang
, Zhang Qianwen
, Feng Biyun
, Gu Shili
, Yao Ru-en
, Yu Tingting
, Ding Yu
, Wang Xiumin
Background: Bardet Biedl syndrome(BBS) is a type of non-motile ciliopathy primarily characterized by retinal dystrophy, obesity, polydactyly, cognitive impairment, urogenital anomalies and renal abnormalities. To date, 26 genes have been reported to be associated with BBS: BBS1-BBS21, IFT74, SCLT1, SCAPER and NPHP1. BBS is genetically heterogeneous with significant clinical overlap with other ciliopathies, further c...