A Case of Pfeiffer Syndrome
Journal of Korean Medical Science
; : 374-378, 2006.
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.
Mots clés
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