Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan

Background: Leri-Weill dyschondrosteosis (LWD) is a pseudoautosomal form of skeletal dysplasia, characterized by abnormal craniofacial phenotype, short stature, and mesomelia of the upper and lower limbs. Methods: We describe two female patients with LWD. Their prime clinical complaints were severe...

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Detalles Bibliográficos
Autores principales: Al Kaissi, Ali, Shboul, Mohammad, Kenis, Vladimir, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631815/
https://www.ncbi.nlm.nih.gov/pubmed/31146331
http://dx.doi.org/10.3390/medicines6020060

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6631815/
https://www.ncbi.nlm.nih.gov/pubmed/31146331
http://dx.doi.org/10.3390/medicines6020060

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