Galloway-Mowat Syndrome in Two Siblings
Journal of the Korean Pediatric Society
; : 1081-1084, 2001.
Article
de Ko
| WPRIM
| ID: wpr-41499
Bibliothèque responsable:
WPRO
ABSTRACT
We report on two Korean siblings with multiple congenital anomalies : microcephaly, gyral abnormality, minor facial anomalies, and congenital nephrotic syndrome. The first infant developed proteinuria at age 3 days. This condition appeared similar to that described by Galloway and Mowat and reviewed by Cooperstone, et al, especially the presence of abnormal gyral patterns. She died at 19 months. The second infant; the brother of the first baby had a very similar condition. These two cases may represent the first cases of Galloway-Mowat syndrome in the Korean population.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Protéinurie
/
Fratrie
/
Microcéphalie
/
Syndrome néphrotique
Limites du sujet:
Humans
/
Infant
langue:
Ko
Texte intégral:
Journal of the Korean Pediatric Society
Année:
2001
Type:
Article