Roussy-Levy Hereditary Areflexic Dystasia (ROULS)

Alias:
Roussy-Levy Syndrome
Roussy-Lévy Syndrome
Hereditary Areflexic Dystasia, Roussy-Lévy Type
Hereditary Areflexic Dystasia, Roussy-Levy Type
Hereditary Motor and Sensory Neuropathy Type I
Charcot-Marie-Tooth Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Roussy-Levy Hereditary Areflexic Dystasia, also known as roussy-levy syndrome, is related to charcot-marie-tooth disease and charcot-marie-tooth disease, demyelinating, type 1b, and has symptoms including back pain, headache and pain. An important gene associated with Roussy-Levy Hereditary Areflexic Dystasia is MPZ (Myelin Protein Zero), and among its related pathways/superpathways are Neural crest differentiation and EGR2 and SOX10-mediated initiation of Schwann cell myelination. The drugs Folic acid and Lipoic acid have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and spinal cord, and related phenotypes are scoliosis and nystagmus

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Infant
--
2
23
19

Medical Symptom

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Gene & Mutation

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Disease Model

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References Literature

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