Pontocerebellar Hypoplasia, Type 3 (PCH3)

Alias:
Pontocerebellar Hypoplasia Type 3
Cerebellar Atrophy with Progressive Microcephaly
Pch3
Pch with Optic Atrophy
Clam
Hypoplasia, Pontocerebellar, Type 3
Pontocerebellar Hypoplasia 3
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基础信息
疾病表征
基因 & 突变
靶点药物
疾病模型
文献报道
桥脑小脑发育不全3型,也称为桥脑小脑发育不全3型,与桥脑小脑发育不全和法洛四联症有关,症状包括肌肉痉挛和癫痫发作。与桥脑小脑发育不全3型有关的重要基因是PCLO(Piccolo Presynaptic Cytomatrix Protein),其相关通路/超级通路包括1p36拷贝数变异综合征。在该疾病的背景下,已提到的药物有地西他滨和索拉非尼。相关组织包括小脑和桥脑,相关表型为癫痫发作和高反射性。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常隐
新生儿
<1/1000000
8
31
4

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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