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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.

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

URI

http://data.loterre.fr/ark:/67375/JVR-N7T2BDLS-K

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