A novel mutation in CDH11, encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndrome

Marco Castori, Claus-Eric Ott, Luigi Bisceglia, Maria Pia Leone, Tommaso Mazza, Stefano Castellana, Jurgen Tomassi, Silvia Lanciotti, Stefan Mundlos, Raoul C. Hennekam, Uwe Kornak, Francesco Brancati

Research output: Contribution to journalArticle

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.
Original languageEnglish
Pages (from-to)2028-2033
Number of pages6
JournalAmerican Journal of Medical Genetics, Part A
Volume176
Issue number9
DOIs
Publication statusPublished - Sep 1 2018

Fingerprint

Cadherins
Mutation
Water
Genes
Exome
Tooth Loss
Cell Shape
Bone Development
Cell Adhesion Molecules
Morphogenesis
Osteogenesis
Intellectual Disability
Hearing
Cell Movement
Siblings
Exons
Up-Regulation
osteoblast cadherin
Cell Line
Skin

Keywords

  • Branchioskeletogenital
  • Elsahy-Waters
  • CDH11
  • Cadherin-11

Cite this

A novel mutation in CDH11, encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndrome. / Castori, Marco; Ott, Claus-Eric; Bisceglia, Luigi; Leone, Maria Pia; Mazza, Tommaso; Castellana, Stefano; Tomassi, Jurgen; Lanciotti, Silvia; Mundlos, Stefan; Hennekam, Raoul C.; Kornak, Uwe; Brancati, Francesco.

In: American Journal of Medical Genetics, Part A, Vol. 176, No. 9, 01.09.2018, p. 2028-2033.

Research output: Contribution to journalArticle

Castori, Marco ; Ott, Claus-Eric ; Bisceglia, Luigi ; Leone, Maria Pia ; Mazza, Tommaso ; Castellana, Stefano ; Tomassi, Jurgen ; Lanciotti, Silvia ; Mundlos, Stefan ; Hennekam, Raoul C. ; Kornak, Uwe ; Brancati, Francesco. / A novel mutation in CDH11, encoding cadherin-11, cause Branchioskeletogenital (Elsahy-Waters) syndrome. In: American Journal of Medical Genetics, Part A. 2018 ; Vol. 176, No. 9. pp. 2028-2033.
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