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Crouzon's syndrome: A review of literature and case report
Crouzon's syndrome is an autosomal dominant disorder with complete penetrance and variable expressivity. Described by a French neurosurgeon in 1912, it is a rare genetic disorder. Crouzon's syndrome is caused by mutation in the fibroblast growth factor receptor 2 (FGFR2) gene. Normally, th...
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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Medknow Publications Pvt Ltd
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3214529/ https://ncbi.nlm.nih.gov/pubmed/22215936 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.86464 |
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