Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia.

ABSTRACT: Very-long-chain fatty acids (VLCFAs) play important roles in membrane structure and cellular signaling, and their contribution to human health is increasingly recognized. Fatty acid elongases catalyze the first and rate-limiting step in VLCFA synthesis. Heterozygous mutations in ELOVL4, the gene encoding one of the elongases, are known to cause macular degeneration in humans and retinal abnormalities in mice. However, biallelic ELOVL4 mutations have not been observed in humans, and murine models with homozygous mutations die within hours of birth as a result of a defective epidermal water barrier. Here, we report on two human individuals with recessive ELOVL4 mutations revealed by a combination of autozygome analysis and exome sequencing. These individuals exhibit clinical features of icht

SUBMITTER: Aldahmesh MA 

PROVIDER: S-EPMC3234380 | biostudies-literature | 2011 Dec

REPOSITORIES: biostudies-literature