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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
Renal coloboma syndrome (RCS), also called papillorenal syndrome, is an autosomal dominant condition characterized by optic nerve… Expand
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2007
2007
PAX2 gene encodes a transcription factor that belongs to the paired-box family of homeotic genes and is widely expressed during… Expand
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2006
2006
Rat male hypogonadism (hgn/hgn) is accompanied by oligomeganephronic hypoplastic kidney (HPK), in which each kidney contains one… 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
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2003
2003
The homeobox transcription factor hepatocyte nuclear factor 1beta (HNF1beta) is a tissue-specific regulator that plays an… Expand
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2001
2001
BACKGROUND Oligomeganephronia (OMN) is a rare congenital and usually sporadic anomaly. It is characterized by bilateral renal… Expand
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1997
1997
We present a patient with features suggestive of Seckel syndrome who was found to be mosaic for ring 4 chromosome. Seckel… Expand
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1994
1994
The histopathology and morphometric findings in two cases of oligomeganephronia occurring in a fetus and a preterm infant are… Expand
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1993
1993
Oligomeganephronia is a rare congenital renal hypoplasia that is characterized histologically by a reduction in the number of… Expand
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1973
1973
The case of a 12-year-old boy with oligomeganephronic renal hypoplasia is reported. On light microscopy the histologic findings… Expand
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