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• W2890870364 endingPage "2033" @default.
• W2890870364 startingPage "2028" @default.
• W2890870364 abstract "Abstract Cadherins are cell‐adhesion molecules that control morphogenesis, cell migration, and cell shape changes during multiple developmental processes. Until now four distinct cadherins have been implicated in human Mendelian disorders, mainly featuring skin, retinal and hearing manifestations. Branchio‐skeleto‐genital (or Elsahy‐Waters) syndrome (BSGS) is an ultra‐rare condition featuring a characteristic face, premature loss of teeth, vertebral and genital anomalies, and intellectual disability. We have studied two sibs with BSGS originally described by Castori et al. in 2010. Exome sequencing led to the identification of a novel homozygous nonsense variant in the first exon of the cadherin‐11 gene ( CDH11 ), which results in a prematurely truncated form of the protein. Recessive variants in CDH11 have been recently demonstrated in two other sporadic patients and a pair of sisters affected by BSGS. Although the function of this cadherin (also termed Osteoblast‐Cadherin) is not completely understood, its prevalent expression in osteoblastic cell lines and up‐regulation during differentiation suggest a specific function in bone formation and development. This study identifies a novel loss‐of‐function variant in CDH11 as a cause of BSGS and supports the role of cadherin‐11 as a key player in axial and craniofacial malformations." @default.
• W2890870364 created "2018-09-27" @default.
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• W2890870364 date "2018-09-01" @default.
• W2890870364 modified "2023-10-04" @default.
• W2890870364 title "A novel mutation in<i>CDH11</i>, encoding cadherin‐11, cause Branchioskeletogenital (Elsahy‐Waters) syndrome" @default.
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• W2890870364 doi "https://doi.org/10.1002/ajmg.a.40379" @default.
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