A carregar...
Seizures as an Atypical Feature of Beal’s Syndrome
Congenital contractural arachnodactyly, commonly known as Beal’s syndrome, is an extremely rare genetic disorder caused by mutations in the fibrillin-2 (FBN2) gene located on chromosome 5q23. It is an autosomal dominant inherited connective tissue disorder characterised by a Marfan-like body habitus...
Na minha lista:
| Publicado no: | Sultan Qaboos Univ Med J |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Sultan Qaboos University Medical Journal, College of Medicine & Health Sciences
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4996306/ https://ncbi.nlm.nih.gov/pubmed/27606123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18295/squmj.2016.16.03.021 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|