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Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus
Crouzon syndrome is one of the most common craniofacial syndromes and is inherited as autosomal dominant with variable expression. We report an 11 and a half-year-old boy with Crouzon syndrome with severe growth retardation. He had hydrocephalus since infancy and recently suffered from frequent dizz...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Hindawi Publishing Corporation
2010
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2878673/ https://ncbi.nlm.nih.gov/pubmed/20585360 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2010/876514 |
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