Neurocutaneous disorders in children

Curr Opin Pediatr. 1993 Aug;5(4):436-40. doi: 10.1097/00008480-199308000-00011.

Abstract

Neurocutaneous syndromes are disorders with cutaneous and neurologic anomalies. Some of these disorders are hereditary. This review summarizes the advances in this field and the recent results obtained in clinical and scientific research on the following syndromes: neurofibromatosis type 1, tuberous sclerosis, Gorlin-Goltz syndrome (nevoid basal cell carcinoma syndrome), Sjögren-Larsson syndrome, trichothiodystrophy, incontinentia pigmenti, CHILD (congenital hemidysplasia with ichthyosiform nevus and limb defects) syndrome, Menkes' syndrome, encephalocraniocutaneous lipomatosis, Proteus syndrome, Sturge-Weber syndrome, and so-called hypomelanosis of lto.

Publication types

  • Review

MeSH terms

  • Basal Cell Nevus Syndrome
  • Child
  • Humans
  • Incontinentia Pigmenti
  • Menkes Kinky Hair Syndrome
  • Nervous System Diseases* / etiology
  • Neurofibromatosis 1
  • Proteus Syndrome
  • Sjogren-Larsson Syndrome
  • Skin Diseases* / etiology
  • Sturge-Weber Syndrome
  • Tuberous Sclerosis