Loading...
Apert syndrome: A case report and review of the literature
Apert syndrome is the rare acrocephalosyndactyly syndrome type 1, characterized by craniosynostosis, severe syndactyly of hands and feet, and dysmorphic facial features. It demonstrates autosomal dominant inheritance assigned to mutations in the fibroblast growth factor receptor gene. Presently desc...
Saved in:
| Published in: | North Clin Istanb |
|---|---|
| Main Author: | |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Kare Publishing
2016
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5206464/ https://ncbi.nlm.nih.gov/pubmed/28058401 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14744/nci.2015.30602 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|