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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Hindawi Publishing Corporation
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878673/ https://www.ncbi.nlm.nih.gov/pubmed/20585360 http://dx.doi.org/10.1155/2010/876514 |