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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Detalles Bibliográficos
Autores principales: Dahan-Oliel, Noémi, Dieterich, Klaus, Rauch, Frank, Bardai, Ghalib, Blondell, Taylor N., Gustafson, Anxhela Gjyshi, Hamdy, Reggie, Latypova, Xenia, Shazand, Kamran, Giampietro, Philip F., van Bosse, Harold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391526/
https://www.ncbi.nlm.nih.gov/pubmed/34440395
http://dx.doi.org/10.3390/genes12081220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391526/
https://www.ncbi.nlm.nih.gov/pubmed/34440395
http://dx.doi.org/10.3390/genes12081220

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