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Sneddon syndrome

Synonyms
Cerebro-vascular lesions and livedo reticularis; Idiopathic livedo reticularis with systemic involvement; Livedo reticularis and cerebrovascular accidents; Sneddon's syndrome
Modes of inheritance
Autosomal dominant inheritance (Orphanet)
Not genetically inherited (Orphanet)

Summary

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). [from OMIM]

Available tests

24 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (24 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ADGF, CECR1, IDGFL, PAN, SNEDS, VAIHS, ADA2
    Summary: adenosine deaminase 2

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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