Isolated Childhood Apraxia of Speech

Alias:
Speech and Language Disorder with Orofacial Dyspraxia
Isolated Developmental Verbal Dyspraxia
Pure Childhood Apraxia of Speech
Isolated Cas
Pure Cas
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Isolated Childhood Apraxia of Speech, also known as speech and language disorder with orofacial dyspraxia, is related to foxp2-related speech and language disorder and toe syndactyly, telecanthus, and anogenital and renal malformations. An important gene associated with Isolated Childhood Apraxia of Speech is FOXP2 (Forkhead Box P2). Affiliated tissues include tongue and brain, and related phenotypes are delayed speech and language development and abnormality of speech or vocalization
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Child
<1/1000000
3
20
19

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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Comparison
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