A carregar...
Clinical characteristics of Crouzon syndrome
Crouzon syndrome (CS) is an genetic disorder with autosomal dominant inheritance caused by mutation of the gene for fibroblast growth factor receptor 2 (FGFR2) was described as one of the varieties of craniosynostosis. In this presented case, premature closure of the sutures had caused restricted sk...
Na minha lista:
| Publicado no: | Oman J Ophthalmol |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2017
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5516458/ https://ncbi.nlm.nih.gov/pubmed/28757702 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0974-620X.209111 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|