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Updated: May 11, 2026

Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease
Published on: February 3, 2012
Reporte de caso: Nefropatía neonatal con apariencia quística en un niño portador de una variante de WT1
Tuyen Thi Thanh Nguyen1,2, Quynh Thuy Huong Tran3, Huong Thi Thanh Nguyen1
1Neonatalogy 2 - Metabolism - Genetics Department, Children's Hospital 1, Ho Chi Minh City, Vietnam.
Una rara mutación del gen WT1 (p.Arg467Gln) causó insuficiencia renal neonatal grave y una apariencia de riñón quístico en un bebé. Este hallazgo destaca los potentes efectos de las variantes de WT1 en la nefropatía relacionada con el tumor de Wilms.
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