Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Término preferido
Sjogren-Larsson Syndrome
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- 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
En otras lenguas
-
francés
-
Déficit en déshydrogénase des aldéhydes gras
URI
http://data.loterre.fr/ark:/67375/JVR-N7T2BDLS-K
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