Pfeiffer type 1 syndrome: a genetically proven case report
IJCN-Iranian Journal of Child Neurology. 2008; 2 (3): 61-65
em Inglês
| IMEMR
| ID: emr-86741
ABSTRACT
Pfeiffer Syndrome is as rare as Apert syndrome in the Western population. This condition is very rare in the Asian population. At the best of our knowledge this is the first genetically proven case report from Iran. The authors report with a review of literature, the case of a infant with Pfeiffer syndrome, manifested by Lacunar skull, ventriculomegaly, bicoronal craniosynostosis, frontal bossing, shallow orbits, parrot-like nose, umbilical hernia, broad and medially deviated great toes
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Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Acrocefalossindactilia
/
Craniossinostoses
Tipo de estudo:
Relato de Casos
Limite:
Humanos
/
Masculino
Idioma:
Inglês
Revista:
Iran. J. Child Neurol.
Ano de publicação:
2008
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