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Descriptor English: Sneddon Syndrome
Descriptor Spanish: Síndrome de Sneddon
Descriptor síndrome de Sneddon
Entry term(s) livedo reticulares con afectación sistémica
síndrome de Sneddon-Champion
Scope note: Arteriopatía sistémica no inflamatoria que ocurre principalmente en mujeres de mediana edad y que se caracteriza por la asociación de LIVEDO RETICULAR, INFARTO CEREBRAL trombótico múltiple, ENFERMEDAD CORONARIA e HIPERTENSIÓN. También puede haber aumento de los títulos de anticuerpos antifosfolipídicos (ver también SÍNDROME ANTIFOSFOLIPÍDICO), valvulopatía cardíaca, ACCIDENTE ISQUÉMICO TRANSITORIO, CONVULSIONES, DEMENCIA e isquemia crónica de las extremidades. El examen anatomopatológico de las arterias afectadas revela fibrosis no inflamatoria de la adventicia, trombosis y cambios en la media. (Traducción libre del original: 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). Las mutaciones en el gen CECR1 (proteína ADA2 humana) se asocian al síndrome de Sneddon.
Descriptor Portuguese: Síndrome de Sneddon
Descriptor French: Syndrome de Sneddon
Entry term(s): Livedo Reticularis And Cerebrovascular Accidents
Livedo Reticularis, Systemic Involvement
Sneddon Champion Syndrome
Sneddon-Champion Syndrome
Syndrome, Sneddon
Syndrome, Sneddon-Champion
Tree number(s): C10.228.140.300.750
C14.907.253.774
C17.800.862.775
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D018860
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). Mutations in the CECR1 gene (ADA2 protein, human) are associated with Sneddon syndrome.
Annotation: do not confuse with SNEDDON-WILKINSON DISEASE see SKIN DISEASES, VESICULOBULLOUS
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Cerebrovascular Disorders (1983-1995)
Skin (1979-1983)
Skin Diseases, Vascular (1993-1995)
Public MeSH Note: 1996
History Note: 1996
DeCS ID: 32608
Unique ID: D018860
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1996/01/01
Date of Entry: 1994/12/27
Revision Date: 2012/07/03
Sneddon Syndrome - Preferred
Concept UI M0028214
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). Mutations in the CECR1 gene (ADA2 protein, human) are associated with Sneddon syndrome.
Preferred term Sneddon Syndrome
Entry term(s) Livedo Reticularis And Cerebrovascular Accidents
Livedo Reticularis, Systemic Involvement
Sneddon Champion Syndrome
Sneddon-Champion Syndrome
Syndrome, Sneddon
Syndrome, Sneddon-Champion



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