Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations


Chernin G., Vega-Warner V., Schoeb D. S. , Heeringa S. F. , Ovunc B., Saisawat P., ...Daha Fazla

CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.5, ss.1655-1662, 2010 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 5 Konu: 9
  • Basım Tarihi: 2010
  • Doi Numarası: 10.2215/cjn.09351209
  • Dergi Adı: CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
  • Sayfa Sayıları: ss.1655-1662

Özet

Background and objectives: The risk of developing Wilms tumor (WT) can be present or absent in patients with nephrotic syndrome (NS) caused by WT1 mutations. Here, the genotype/phenotype correlation regarding the outcome and risk for WT in 52 patients from 51 families with NS due to WT1 mutations is described.