Cowden Syndrome (CD)

Cowden Syndrome(来自ICD-11)
别称:
Cowden Disease
Multiple Hamartoma Syndrome
Lhermitte-Duclos Disease
Cowden's Disease
Dysplastic Gangliocytoma of Cerebellum
Hamartoma Syndrome, Multiple
Cowden's Syndrome
Mham
Cs
Cd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cowden Syndrome, also known as cowden disease, is related to cowden syndrome 1 and cowden syndrome 4, and has symptoms including seizures, action tremor and cerebellar ataxia. An important gene associated with Cowden Syndrome is PTEN (Phosphatase And Tensin Homolog), and among its related pathways/superpathways are Signal Transduction and Prolactin Signaling. The drugs Everolimus and Temsirolimus have been mentioned in the context of this disorder. Affiliated tissues include thyroid and breast, and related phenotypes are generalized hyperkeratosis and palmoplantar keratoderma
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相关ID:
MESH:D006223

基础信息

遗传方式
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参考文献
MALACARDS
AD
All ages
1-9/1000000
89
1321
54

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靶点药物

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MGI
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