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Concept information

Preferred term

Homocystinuria  

Type

  • Topical Descriptor

Entry terms

  • Cystathionine beta Synthase Deficiency Disease
  • Cystathionine beta-Synthase Deficiency Disease

Scope note

  • Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979)

History note

  • 1969(1967)

In other languages

URI

http://www.yso.fi/onto/mesh/D006712

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