Foxg1 Syndrome

Alias:
Foxg1-Related Epileptic-Dyskinetic Encephalopathy
Foxg1-Related Disorder
Foxg1 Disorder
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Foxg1 Syndrome, also known as foxg1-related epileptic-dyskinetic encephalopathy, is related to foxg1 syndrome due to 14q12 microdeletion and foxg1 syndrome due to intragenic alteration, and has symptoms including athetosis, constipation and muscle spasticity. An important gene associated with Foxg1 Syndrome is FOXG1 (Forkhead Box G1). Affiliated tissues include brain and eye, and related phenotypes are hypotonia and dyskinesia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Newborn
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1
10
5

Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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