Smith-Magenis Syndrome (SMS)

Alias:
Sms
17p11.2 Microdeletion Syndrome
Chromosome 17p11.2 Deletion Syndrome
Chromosome 17p Deletion Syndrome
Stiff Person Spectrum Disorder
Moersch-Woltman Syndrome
Stiff Man Syndrome
17p11.2 Monosomy
Sps
Deletion 17p Syndrome
Partial Monosomy 17p
17p- Syndrome
Del(17)
P11.2
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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
史密斯-马根尼斯综合症,也被称为sms,与波托基-卢普斯基综合症和自闭症谱系障碍有关,症状包括嘶哑和睡眠障碍。与史密斯-马根尼斯综合症有关的重要基因是RAI1(视黄酸诱导1),其相关通路/超级通路包括史密斯-马根尼斯和波托基-卢普斯基综合症拷贝数变异。在该疾病的背景下,已提到过泼马利多米德和地塞米松。附属组织包括肾脏和眼睛,相关表型为智力障碍和前额突出。
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
常显
新生儿
1-9/1000000
52
493
104

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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