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Apert Syndrome: Report of a rare congenital malformation
A rare case of an adult male with malformation of the skull, face, hands and feet called acrocephalosyndactly or Apert syndrome is presented. Its probable cause, features and treatment is discussed. It is a unique case who survived upto the age of 32 years without any operative intervention and adju...
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| Publicat a: | Pak J Med Sci |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Professional Medical Publications
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5510146/ https://ncbi.nlm.nih.gov/pubmed/28811814 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12669/pjms.333.12878 |
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