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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...
Tallennettuna:
| Julkaisussa: | Oman J Ophthalmol |
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| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications & Media Pvt Ltd
2017
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| Aiheet: | |
| Linkit: | 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 |
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