Definitions for sjogren-larsson syndrome
This page provides all possible meanings and translations of the word sjogren-larsson syndrome
Sjögren–Larsson syndrome is an autosomal recessive form of ichthyosis apparent at birth. Sjögren–Larsson syndrome is a rare autosomal, recessive, neurocutaneous disease. This disease can be identified by a triad of medical disorders. The first is ichthyosis, which is a buildup of skin to form a scale-like covering that causes dry skin and other problems. The second identifier is spastic paraplegia which is characterized by leg spasms. The final identifier is mental retardation. The gene of SLS is found on chromosome 17. In order for a child to receive SLS both parents must be carriers of the SLS gene. If they are carriers their child has a ¼ chance of getting the disease. In 1957 Sjogren and Larsson proposed that the Swedes with the disease all descended from a common ancestor 600 years ago. Today only 1% of Northern Sweden's population has this disease.
U.S. National Library of Medicine
An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism.
Find a translation for the sjogren-larsson syndrome definition in other languages:
Select another language:
Discuss these sjogren-larsson syndrome definitions with the community:
Use the citation below to add this definition to your bibliography:
"sjogren-larsson syndrome." Definitions.net. STANDS4 LLC, 2014. Web. 11 Mar. 2014. <http://www.definitions.net/definition/sjogren-larsson syndrome>.