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Oligomeganephronia

Congenital renal hypoplasia characterized by small kidneys; reduced nephron number; tubular and glomerular hypertrophy.(NICHD)
National Institutes of Health

Papers overview

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Review
2011
Review
2011
  • L. Schimmenti
  • European Journal of Human Genetics
  • 2011
  • Corpus ID: 35641595
Renal coloboma syndrome (RCS), also called papillorenal syndrome, is an autosomal dominant condition characterized by optic nerve… Expand
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2011
2011
Oligomeganephronia is classified as a subgroup of renal hypoplasia, characterized by histopathologic abnormalities which progress… Expand
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2011
2011
A 23 year-old male was investigated for hypertension, moderate renal insufficiency, persistent proteinuria and bilateral small… Expand
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Review
2004
Review
2004
The number of pregnancies in immunosuppressed women has increased during the recent years and this has become a major part of the… Expand
Highly Cited
2003
Highly Cited
2003
The homeobox transcription factor hepatocyte nuclear factor 1beta (HNF1beta) is a tissue-specific regulator that plays an… Expand
Highly Cited
2001
Highly Cited
2001
BACKGROUND Oligomeganephronia (OMN) is a rare congenital and usually sporadic anomaly. It is characterized by bilateral renal… Expand
1993
1993
Oligomeganephronia is a rare congenital renal hypoplasia that is characterized histologically by a reduction in the number of… Expand
1977
1977
Abstract A patient with clinical, laboratory, and biopsy findings of bilateral renal hypoplasia with oligomeganephronia is… Expand
1973
1973
The case of a 12-year-old boy with oligomeganephronic renal hypoplasia is reported. On light microscopy the histologic findings… Expand
1970
1970
The syndrome of congenital bilateral renal hypoplasia with hypertrophy of nephrons has been well documented in the French… Expand