Autosomal Recessive Progressive External Ophthalmoplegia (ARPEO)

Alias:
Arpeo
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Autosomal Recessive Progressive External Ophthalmoplegia, also known as arpeo, is related to progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 and mitochondrial dna depletion syndrome, and has symptoms including ophthalmoplegia An important gene associated with Autosomal Recessive Progressive External Ophthalmoplegia is POLG (DNA Polymerase Gamma, Catalytic Subunit). Affiliated tissues include eye and skeletal muscle, and related phenotypes are dysphagia and facial palsy
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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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2
15
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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