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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Pak J Med Sci |
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| Κύριοι συγγραφείς: | , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Professional Medical Publications
2017
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| Θέματα: | |
| Διαθέσιμο Online: | 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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