Congenital microcephaly and infantile nephrotic syndrome ? a case report

descriptionPublicationkeyboard_double_arrow_right Article 01 Feb 1994 English Publisher:Springer Science and Business Media LLCJournal:Pediatric Nephrology, volume 8, pages 72-73 (issn: 0931-041X, eissn: 1432-198X,

Copyright policy )

Authors: F, Yalçinkaya; N, Tümer; M, Ekim; S, Kuyucu; N, Cakar; C, Ensari;

doi: 10.1007/bf00868267

pmid: 8142231

Congenital microcephaly and infantile nephrotic syndrome ? a case report

- Summary
- Subjects
- Metrics

Abstract

A 22-month-old girl with nephrotic syndrome and microcephaly is described. She had dysmorphic facies and psychomotor retardation. Her parents were first-degree relatives and one of her siblings had died with nephrotic syndrome and renal failure in infancy. An autosomal recessive inheritance is suggested. The diagnosis of this rare combination is discussed and the relevant literature is reviewed.

Related Organizations

Ankara University
Turkey

Keywords

Nephrotic Syndrome, Prednisolone, Microcephaly, Humans, Infant, Female, Psychomotor Disorders, Cyclophosphamide

Impact byBIP!

	selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	14
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Average
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Top 10%
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Average