Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Ichthyosis
Preferred term
Sjogren-Larsson Syndrome
Type
-
Topical Descriptor
Broader concept
Entry terms
- Congenital Icthyosis Mental Retardation Spasticity Syndrome
- FALDH Deficiency
- Fatty Alcohol:NAD+ Oxidoreductase Deficiency
- Fatty Aldehyde Dehydrogenase Deficiency
- Fatty Aldehyde Dehydrogenase Deficiency Disease
- Ichthyosis Oligophrenia Syndrome
- Ichthyosis, Spastic Neurologic Disorder, and Oligophrenia
- Sjögren-Larsson Syndrome
Note
- do not confuse with SJOGREN'S SYNDROME; in titles & translations use diacritic: Sjögren-Larsson
Scope note
- 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.
History note
- 1991; use ICHTHYOSIS 1984-1990
In other languages
-
Finnish
-
Sjögren-Larsson
-
Sjögren-Larssonin iktyoosi
-
Sjögren-Larssonin kalansuomusairaus
-
Sjögren-Larssonin kalansuomutauti
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Sjögren-Larssonin syndrooma
-
Syndroma Sjögren-Larsson
-
Swedish
URI
http://www.yso.fi/onto/mesh/D016111
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