Pelizaeus-Merzbacher Disease (PMD)

Alias:
Pmd
Pelizaeus-Merzbacher Brain Sclerosis
Hld1
Sudanophilic Leukodystrophy, Paelizeus-Merzbacher Type
Diffuse Familial Brain Sclerosis
Cockayne-Pelizaeus-Merzbacher Disease
Leukodystrophy, Hypomyelinating, 1
Leukodystrophy, Sudanophilic
Sudanophilic Leukodystrophy Paelizeus-Merzbacher Type
Pelizaeus-Merzbacher Disease, Connatal Form
Pelizaeus-Merzbacher Disease, Null Syndrome
Diffuse Cerebral Sclerosis of Schilder
Pelizaeus Merzbacher Brain Sclerosis
Pelizaeus-Merzbacher Disease Type Ii
Hypomyelinating Leukodystrophy, 1
Hypomyelinating Leukodystrophy 1
Brain Sclerosis Diffuse Familial
Leukodystrophy Hypomyelinating 1
Sudanophilic Leukodystrophy
Plp1 Null Syndrome
Null Syndrome
Connatal Pmd
Severe Pmd
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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
佩里扎尤斯-梅尔泽巴赫病,也称为pmd,与佩里扎尤斯-梅尔泽巴赫样病和白质营养不良,低髓鞘化,3有关,其症状包括共济失调,肌肉痉挛和癫痫发作。与佩里扎尤斯-梅尔泽巴赫病有关的重要基因是PLP1(蛋白脂蛋白1),其相关通路/超级通路包括神经嵴分化和少突胶质细胞特化和分化,导致中枢神经系统髓鞘成分。在该疾病的背景下提到了泼尼松和泼尼松酸。附属组织包括脊髓和大脑,相关表型为痉挛和脊柱侧弯。
Related ID:
MESH:D020371
ICD11:1313582105

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
X显
X染色体
X隐
新生儿
<1/1000000
22
105
79

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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