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- W2024793245 abstract "We report on two Chinese female infants with multiple congenital anomalies: microcephaly, apparent porencephaly or encephalomalacia, developmental delay, minor facial anomalies, and contractural arachnodactyly. In the first patient, focal glomerulosclerosis was diagnosed histologically by percutaneous renal biopsy due to proteinuria with hematuria. Congenital hypothyrodism presenting with markedly low T3 and T4 was also noted. She died at age 5 months. The second patient had a very similar condition but less severe brain and kidney malformations. A variant of Galloway-Mowat syndrome is suspected. © 1995 Wiley-Liss, Inc." @default.
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- W2024793245 date "1995-09-11" @default.
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- W2024793245 title "Galloway-Mowat syndrome in Taiwan" @default.
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- W2024793245 doi "https://doi.org/10.1002/ajmg.1320580310" @default.
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