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Sneddon syndrome

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Description

Sneddon syndrome is a noninflammatory arteriopathy characterized by onset of livedo reticularis in the second decade and onset of cerebrovascular disease in early adulthood (summary by Bras et al., 2014). Livedo reticularis occurs also with polyarteritis nodosa, systemic lupus erythematosus, and central thrombocythemia, any one of which may be accompanied by cerebrovascular accidents (Bruyn et al., 1987).

OMIM

  • Mode of Inheritance

  • Sporadic
  • Autosomal recessive inheritance

VARIANTS

5

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Genes

External Links

  • OMIM

    182410

  • Orphanet

    820

  • HPO
  • Medgen

    C0282492

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