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A Case of Pfeiffer Syndrome
Article in English | WPRIM (Western Pacific) | ID: wpr-12242
Responsible library: 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.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Acrocephalosyndactylia / Korea Limits: Female / Humans / Infant, Newborn Country/Region as subject: Asia Language: English Journal: Journal of Korean Medical Science Year: 2006 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Acrocephalosyndactylia / Korea Limits: Female / Humans / Infant, Newborn Country/Region as subject: Asia Language: English Journal: Journal of Korean Medical Science Year: 2006 Document type: Article
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