WebJan 8, 2024 · Bardet-Biedl syndrome (BBS) is a rare ciliopathic human genetic disorder with mainly an autosomal recessive inheritance. BBS phenotype develops over the years and … WebSep 10, 2002 · Insufficient manifestations of overlapping syndromes, such as Bardet-Biedl syndrome (BBS) for a diagnosis of this syndrome or another condition Family history …

Bardet-Biedl Syndrome - Symptoms, Causes, Treatment

WebOct 1, 2003 · As with other leading technologies, BBS has evolved over the years to become more effective, as well as more agile and adaptable by a growing range of industries, … WebAug 3, 2013 · At cancer diagnosis, 74 (9.3 %) women out of 800 were BBs users. Median age was 62 years in BB users and 59 years in non-users ( P = 0.02). BB users and non-users were similarly distributed by all tumor characteristics. The 5-year cumulative incidence of BC-related events was 13.6 % in BB users and 27.9 % in non-users ( P = 0.02). the product manager handbook

Allelic overload and its clinical modifier effect in Bardet-Biedl ...

WebBardet–Biedl syndrome (BBS), sometimes known as Laurence–Moon–Bardet-Biedl syndrome, is a rare autosomal recessive ciliopathy characterized by rod-cone dystrophy, learning difficulties, polydactyly, obesity, genital malformations, and renal abnormalities. In the 1880s, a family with retinitis pigmentosa, obesity, and intellectual ... Web46 rows · Bardet-Biedl Syndrome (BBS) is a rare (prevalence 1 in 125,000 to 160,000) highly pleiotropic autosomal recessive disorder associated with variable phenotypes. 110 Main … WebAug 26, 2016 · Clinical Findings BBS is a ciliopathy with protean manifestations. Cilia gene mutations can cause a range of clinical conditions with retinal and renal dysfunction as common recurrent features. the product market is where