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Sneddon Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ Sneddon Syndrome 28 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sneddon Syndrome 28 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Sneddon Syndrome 28 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | |
Annotation: | do not confuse with SNEDDON-WILKINSON DISEASE see SKIN DISEASES, VESICULOBULLOUS
X |
History note: | |
historyNote*: | 1996
X |
publicMeSHNote*: | 1996
X |
Scope note: | A systemic non-inflammatory arteriopathy primarily of middle-aged females characterized by the association of livedo reticularis, multiple thrombotic CEREBRAL INFARCTION; CORONARY DISEASE, and HYPERTENSION. Elevation of antiphospholipid antibody titers (see also ANTIPHOSPHOLIPID SYNDROME), cardiac valvulopathy, ISCHEMIC ATTACK, TRANSIENT; SEIZURES; DEMENTIA; and chronic ischemia of the extremities may also occur. Pathologic examination of affected arteries reveals non-inflammatory adventitial fibrosis, thrombosis, and changes in the media. (From Jablonski, Dictionary of Syndromes & Eponymic Diseases, 2d ed; Adams et al., Principles of Neurology, 6th ed, p861; Arch Neurol 1997 Jan;54(1):53-60)
X |
activeMeSHYear*: | |
dateCreated*: | 1994-12-27X |
dateEstablished*: | 1996-01-01X |
dateRevised*: | 1999-12-13X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | TGCX |
Type: | |
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Labels and equivalent concepts: | Sneddonin oireyhtymä (fi) XSneddon-Champion Syndrome (en, replaced) Livedo Reticularis, Systemic Involvement (en, replaced) Síndrome de Sneddon (es) Sneddon-Syndrom (de) Sneddonův syndrom (cs) Livedo Reticularis de Compromiso Sistémico (es, replaced) Síndrome de Sneddon-Champion (es, replaced) Sneddon-Champion-Syndrom (de, replaced) Livedo racemosa generalisata (de, replaced) |
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