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A Case of Pfeiffer Syndrome
Article de En | WPRIM | ID: wpr-12242
Bibliothèque responsable: WPRO
ABSTRACT
Pfeiffer Syndrome is as rare as Apert syndrome in the Western population. This condition is very rare in the Asian population and has not been previously reported in Korea. The authors report with a review of literature the case of a newborn baby with Pfeiffer syndrome, manifested by bicoronal craniosynostosis, broad thumbs, and big toes. The infant also had bilateral syndactyly of the fingers and toes, mild proptosis, choanal hypoplasia and maxillary hypoplasia.
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Texte intégral: 1 Indice: WPRIM Sujet Principal: Acrocéphalosyndactylie / Corée Limites du sujet: Female / Humans / Newborn Pays comme sujet: Asia langue: En Texte intégral: Journal of Korean Medical Science Année: 2006 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Acrocéphalosyndactylie / Corée Limites du sujet: Female / Humans / Newborn Pays comme sujet: Asia langue: En Texte intégral: Journal of Korean Medical Science Année: 2006 Type: Article