Congenital microcephaly and infantile nephrotic syndrome--a case report

Pediatr Nephrol. 1994 Feb;8(1):72-3. doi: 10.1007/BF00868267.

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.

Publication types

  • Case Reports

MeSH terms

  • Cyclophosphamide / therapeutic use
  • Female
  • Humans
  • Infant
  • Microcephaly / complications*
  • Nephrotic Syndrome / complications*
  • Nephrotic Syndrome / drug therapy
  • Prednisolone / therapeutic use
  • Psychomotor Disorders / complications
  • Psychomotor Disorders / genetics

Substances

  • Cyclophosphamide
  • Prednisolone