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Arterial calcification of infancy [Supplementary Concept]

A severe hereditary autosomal recessive disorder characterized by calcification of the internal elastic lamina of muscular arteries and STENOSIS due to myointimal proliferation. It is often fatal within the first 6 months of life because of MYOCARDIAL ISCHEMIA resulting in refractory HEART FAILURE. Mutations in the ENPP1 gene have been identified. OMIM: 208000

Date introduced: August 25, 2010

MeSH Unique ID: C537440

Heading Mapped to:

Entry Terms:

  • Occlusive infantile arteriopathy
  • Idiopathic infantile arterial calcification
  • Generalized arterial calcification in infancy
  • Arterial Calcification, Generalized, Of Infancy
  • Arteriopathy, Occlusive Infantile
  • GACI
  • Arterial Calcification, Idiopathic Infantile

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