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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... |
