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Concept information

Preferred term

Menkes Kinky Hair Syndrome  

Type

  • Topical Descriptor

Entry terms

  • Congenital Hypocupremia
  • Congenital Hypocupremias
  • Copper Deficiencies, X-Linked
  • Copper Deficiency, X-Linked
  • Copper Transport Disease
  • Copper Transport Diseases
  • Deficiencies, X-Linked Copper
  • Deficiency, X-Linked Copper
  • Disease, Copper Transport
  • Diseases, Copper Transport
  • Diseases, Kinky Hair
  • Diseases, Menkes'
  • Diseases, Steely Hair
  • Disease, Steely Hair
  • Hair Diseases, Kinky
  • Hair Diseases, Steely
  • Hypocupremia, Congenital
  • Hypocupremias, Congenital
  • Kinky Hair Disease
  • Kinky Hair Diseases
  • Kinky Hair Syndrome
  • Menkea Syndrome
  • Menkea Syndromes
  • Menkes Disease
  • Menkes' Disease
  • Menkes' Diseases
  • Menkes Syndrome
  • Steely Hair Disease
  • Steely Hair Diseases
  • Steely Hair Syndrome
  • Steely Hair Syndromes
  • Syndrome, Menkea
  • Syndromes, Menkea
  • Syndromes, Steely Hair
  • Syndrome, Steely Hair
  • Transport Disease, Copper
  • Transport Diseases, Copper
  • X-Linked Copper Deficiencies
  • X Linked Copper Deficiency
  • X-Linked Copper Deficiency

Scope note

  • An inherited disorder of copper metabolism transmitted as an X-linked trait and characterized by the infantile onset of HYPOTHERMIA, feeding difficulties, hypotonia, SEIZURES, bony deformities, pili torti (twisted hair), and severely impaired intellectual development. Defective copper transport across plasma and endoplasmic reticulum membranes results in copper being unavailable for the synthesis of several copper containing enzymes, including PROTEIN-LYSINE 6-OXIDASE; CERULOPLASMIN; and SUPEROXIDE DISMUTASE. Pathologic changes include defects in arterial elastin, neuronal loss, and gliosis. (From Menkes, Textbook of Child Neurology, 5th ed, p125)

History note

  • 2000(1977)

In other languages

URI

http://www.yso.fi/onto/mesh/D007706

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