Autosomal recessive polycystic kidney disease: the clinical experience in North America.

@article{GuayWoodford2003AutosomalRP,
  title={Autosomal recessive polycystic kidney disease: the clinical experience in North America.},
  author={L. M. Guay-Woodford and Renee Ann Desmond},
  journal={Pediatrics},
  year={2003},
  volume={111 5 Pt 1},
  pages={1072-80}
}
OBJECTIVE We designed a longitudinal clinical database for autosomal recessive polycystic kidney disease (ARPKD), recruited patients from pediatric nephrology centers in the United States and Canada, and examined their clinical morbidities and survival characteristics. We initially targeted enrollment to children who were born and diagnosed after January 1, 1990, so as to capture a cohort that is representative of ARPKD patients born in the last decade. When a significant number of older ARPKD… CONTINUE READING
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PKHD 1 , the polycystic kidney and hepatic disease 1 gene , encodes a novel large protein containing multiple IPT domains and PbH 1 repeats

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Prenatal diagnosis of autosomal recessive polycystic kidney disease ( ARPKD ) : molecular genetics , clinical experience , and fetal morphology

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