Apert's Syndrome: A Rare Case Report
Apert's syndrome /Acrocephalosyndactyly is a rare, congenital disorder characterized by craniosynostosis, midfacial malformations and symmetrical syndactyly. It is caused by a genetic mutation in the FGFR2 gene on chromosome 10. Although the syndrome has typical clinical features, the relative...
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| Formato: | Libro |
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Wolters Kluwer Medknow Publications,
2010-01-01T00:00:00Z.
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| Número de Clasificación: |
A1234.567 |
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