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Rolandic Epilepsy-Speech Dyspraxia Syndrome

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Rolandic Epilepsy-Speech Dyspraxia Syndrome is related to childhood electroclinical syndrome and speech disorder. An important gene associated with Rolandic Epilepsy-Speech Dyspraxia Syndrome is GRIN2A (Glutamate Ionotropic Receptor NMDA Type Subunit 2A). Related phenotypes are seizure and delayed speech and language development
Related ID：
MALACARDS：RLN004

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XLR
AD
XL
Unknown
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2
18
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RLN004

Medical Symptom

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Description
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Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Related Drugs

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CAS Number
Status
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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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