Síndrome de pfeiffer: a propósito de un caso
Pfeiffer syndrome (PS) is a rare genetical disorder, originally described by Pfeiffer in 1964, and is characterized by craniosynostosis, regressed midface, syndactyly of hands and feet, and broad thumbs and big toes, with a wide range of variable severity. We report a case with a review of liter...
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| Autores principales: | , , , , , |
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| Formato: | Artículo |
| Lenguaje: | español |
| Publicado: |
Universidad de Salamanca
2011
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| Materias: | |
| Acceso en línea: | https://dialnet.unirioja.es/servlet/oaiart?codigo=3680364 |
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| Sumario: | Pfeiffer syndrome (PS) is a rare genetical disorder, originally described by Pfeiffer in
1964, and is characterized by craniosynostosis, regressed midface, syndactyly of
hands and feet, and broad thumbs and big toes, with a wide range of variable
severity. We report a case with a review of literature. Obstruction of the upper airway
in relation to the midface hypoplasia is a frequent complication in severe cases to be
assessed and treated early. |
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