Neurodevelopmental Disorder with Absent Language and Variable Seizures (NEDALVS)

Alias:
Ito-Raymond Syndrome
Nedalvs
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Neurodevelopmental Disorder with Absent Language and Variable Seizures, also known as ito-raymond syndrome, is related to cerebellar atrophy, developmental delay, and seizures and visual epilepsy. An important gene associated with Neurodevelopmental Disorder with Absent Language and Variable Seizures is WASF1 (WASP Family Member 1). Affiliated tissues include brain and eye, and related phenotypes are delayed speech and language development and intellectual disability, severe
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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1
8
3

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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