Loading...
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:
| Udgivet i: | Oman J Ophthalmol |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Medknow Publications & Media Pvt Ltd
2017
|
| Fag: | |
| Online adgang: | 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: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|