Neurodevelopmental Disorder with Spastic Diplegia and Visual Defects (NEDSDV)

Alias:
Nedsdv
Severe Intellectual Disability-Progressive Spastic Diplegia Syndrome
Eurodevelopmental Disorder with Spastic Diplegia and Visual Defects
Mental Retardation, Autosomal Dominant 19, Formerly
Mrd19, Formerly
Mrd19
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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
神经发育障碍伴痉挛性截瘫和视觉缺陷,也称为nedsdv,与严重的智力障碍-进行性痉挛性截瘫综合征和常染色体显性智力发育障碍19有关。与神经发育障碍伴痉挛性截瘫和视觉缺陷有关的重要基因是CTNNB1(β-连环蛋白)。附属组织包括皮肤和大脑,相关表型为智力障碍和全球发育延迟。
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
未知
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1
31
14

Medical Symptom

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

Gene & Mutation

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No data available

Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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No Data Found!
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