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Crouzon’s Syndrome: A Rare Genetic Disorder
Crouzon’s syndrome, also known as brachial arch 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...
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| Publicado no: | Int J Clin Pediatr Dent |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Jaypee Brothers Medical Publishers
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5233708/ https://ncbi.nlm.nih.gov/pubmed/28127173 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5005/jp-journals-10005-1395 |
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