Actin-Accumulation Myopathy

Alias:
Congenital Myopathy with Excess of Thin Filaments
Actin Accumulation Myopathy
Nemaline Myopathy 3
Actin Myopathy
Actin Filament Aggregate Myopathy
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Actin-Accumulation Myopathy, also known as congenital myopathy with excess of thin filaments, is related to congenital myopathy 2a, typical, autosomal dominant and myopathy, and has symptoms including waddling gait, facial paresis and generalized muscle weakness. An important gene associated with Actin-Accumulation Myopathy is ACTA1 (Actin Alpha 1, Skeletal Muscle). Affiliated tissues include skeletal muscle.
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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1
4
69

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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