Congenital ichthyosis with spastic paraplegia of adult onset.

Journal Article

Two siblings had what we believe to be a unique disorder manifested by stationary congenital ichthyosiform erythroderma coupled with a slowly progressive spastic weakness of adult onset. The disorder was presumably inherited as an autosomal recessive trait. The mechanism by which a genetic mutation would mediate this multiple organ system disorder is unknown.

Full Text

Duke Authors

Cited Authors

  • McNamara, JO; Curran, JR; Itabashi, HH

Published Date

  • October 1, 1975

Published In

Volume / Issue

  • 32 / 10

Start / End Page

  • 699 - 701

PubMed ID

  • 1180734

Pubmed Central ID

  • 1180734

International Standard Serial Number (ISSN)

  • 0003-9942

Digital Object Identifier (DOI)

  • 10.1001/archneur.1975.00490520069011


  • eng

Conference Location

  • United States