Sneddon Syndrome (SNDNS)

Sneddon Syndrome(来自ICD-11)
别称:
Livedo Reticularis-Cerebrovascular Accident Syndrome
Livedo Racemosa-Cerebrovascular Accident Syndrome
Livedo Reticularis and Cerebrovascular Accidents
Ehrmann-Sneddon Syndrome
Sndns
Idiopathic Livedo Reticularis with Systemic Involvement
Sneddon's Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
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References Literature
Sneddon Syndrome, also known as livedo reticularis-cerebrovascular accident syndrome, is related to antiphospholipid syndrome and cerebrovascular disease, and has symptoms including headache, hemiplegia and seizures. An important gene associated with Sneddon Syndrome is ADA2 (Adenosine Deaminase 2). Affiliated tissues include skin and bone, and related phenotypes are vascular skin abnormality and vertigo
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相关ID:
MESH:D018860
ICD11:1474816492

基础信息

遗传方式
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患病率/发病率
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参考文献
MALACARDS
AR
AD
Adult
1-9/1000000
12
62
13

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