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
Language
- eng
Conference Location
- United States