Oligomeganephronia

Renal coloboma syndrome (RCS), also called papillorenal syndrome, is an autosomal dominant condition characterized by optic nerve… Expand

PAX2 gene encodes a transcription factor that belongs to the paired-box family of homeotic genes and is widely expressed during… Expand

Rat male hypogonadism (hgn/hgn) is accompanied by oligomeganephronic hypoplastic kidney (HPK), in which each kidney contains one… Expand

The number of pregnancies in immunosuppressed women has increased during the recent years and this has become a major part of the… Expand

The homeobox transcription factor hepatocyte nuclear factor 1beta (HNF1beta) is a tissue-specific regulator that plays an… Expand

BACKGROUND Oligomeganephronia (OMN) is a rare congenital and usually sporadic anomaly. It is characterized by bilateral renal… Expand

We present a patient with features suggestive of Seckel syndrome who was found to be mosaic for ring 4 chromosome. Seckel… Expand

The histopathology and morphometric findings in two cases of oligomeganephronia occurring in a fetus and a preterm infant are… Expand

Oligomeganephronia is a rare congenital renal hypoplasia that is characterized histologically by a reduction in the number of… Expand

The case of a 12-year-old boy with oligomeganephronic renal hypoplasia is reported. On light microscopy the histologic findings… Expand