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Rev Neurol. 1997 Sep;25 Suppl 3:S238-42.

[Keratotic neurocutaneous syndromes].

[Article in Spanish]

Author information

  • 1Sección de Dermatología, Hospital Universitario Virgen de las Nieves, Granada, España.

Abstract

OBJECTIVE:

To review current knowledge of etiologic, clinic, diagnostic and therapeutic aspects of ichthyotic diseases with neurologic manifestations.

DEVELOPMENT:

Classic keratotic neurocutaneous syndromes including Sjögren-Larsson syndrome, trichotyodystrophy, KID (keratitis, ichthyosis and deafness) syndrome and Rud syndrome, are reviewed. Furthermore, we pay attention to syndromes whose description and study are of current importance: cardiofaciocutaneous syndrome, neutral lipids storage disease with ichthyosis, multiple sulphatase deficiency disease and peroxisomal disorders.

CONCLUSIONS:

Keratotic neurocutaneous syndromes knowledge will help to improve its diagnosis and therapeutic approach.

PMID:
9273168
[PubMed - indexed for MEDLINE]
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