The Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: A Case Series on 12 Children

The Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: A Case Series on 12 Children

Background: Multiple pterygium syndrome (MPS) is a genetically heterogeneous rare form of arthrogryposis multiplex congenita characterized by joint contractures and webbing or pterygia, as well as distinctive facial features related to diminished fetal movement. It is divided into prenatally lethal...

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Bibliographic Details
Main Authors: Noémi Dahan-Oliel, Klaus Dieterich, Frank Rauch, Ghalib Bardai, Taylor N. Blondell, Anxhela Gjyshi Gustafson, Reggie Hamdy, Xenia Latypova, Kamran Shazand, Philip F. Giampietro, Harold van Bosse
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Genes
Subjects:
<i>CHRNG</i>
distal arthrogryposis type 8
Escobar
multiple pterygium syndrome
<i>MYH3</i>
scoliosis
Online Access:https://www.mdpi.com/2073-4425/12/8/1220

Internet

https://www.mdpi.com/2073-4425/12/8/1220

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