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- Roussy–Lévy_syndrome abstract "Roussy–Lévy syndrome, also known as Roussy–Lévy hereditary areflexic dystasia, is a rare genetic disorder of humans that results in progressive muscle wasting. It is caused by mutations in the genes that code for proteins necessary for the functioning of the myelin sheath of the neurons, affecting the conductance of nerve signals and resulting in loss of muscles' ability to move.The condition affects people from infants through adults and is inherited in an autosomal dominant manner. Currently, no cure is known for the disorder.".
- Roussy–Lévy_syndrome icd10 "G60.0".
- Roussy–Lévy_syndrome icd9 "334.3".
- Roussy–Lévy_syndrome omim "180800".
- Roussy–Lévy_syndrome wikiPageID "36308777".
- Roussy–Lévy_syndrome wikiPageLength "9803".
- Roussy–Lévy_syndrome wikiPageOutDegree "55".
- Roussy–Lévy_syndrome wikiPageRevisionID "678481085".
- Roussy–Lévy_syndrome wikiPageWikiLink Anatomical_terms_of_location.
- Roussy–Lévy_syndrome wikiPageWikiLink Areflexia.
- Roussy–Lévy_syndrome wikiPageWikiLink Ataxia.
- Roussy–Lévy_syndrome wikiPageWikiLink Atrophy.
- Roussy–Lévy_syndrome wikiPageWikiLink Autosomal_dominant.
- Roussy–Lévy_syndrome wikiPageWikiLink Category:Autosomal_dominant_disorders.
- Roussy–Lévy_syndrome wikiPageWikiLink Category:Neurogenetic_disorders.
- Roussy–Lévy_syndrome wikiPageWikiLink Charcot–Marie–Tooth_disease.
- Roussy–Lévy_syndrome wikiPageWikiLink Corrective_surgery.
- Roussy–Lévy_syndrome wikiPageWikiLink Corrective_therapy.
- Roussy–Lévy_syndrome wikiPageWikiLink Dejerine–Sottas_disease.
- Roussy–Lévy_syndrome wikiPageWikiLink Dominance_(genetics).
- Roussy–Lévy_syndrome wikiPageWikiLink Electromyography.
- Roussy–Lévy_syndrome wikiPageWikiLink Fibroblast.
- Roussy–Lévy_syndrome wikiPageWikiLink Fibroblasts.
- Roussy–Lévy_syndrome wikiPageWikiLink Foot_drop.
- Roussy–Lévy_syndrome wikiPageWikiLink Gabrielle_Lévy.
- Roussy–Lévy_syndrome wikiPageWikiLink Gene.
- Roussy–Lévy_syndrome wikiPageWikiLink Gene_duplication.
- Roussy–Lévy_syndrome wikiPageWikiLink Genetic_disorder.
- Roussy–Lévy_syndrome wikiPageWikiLink Genetic_mutation.
- Roussy–Lévy_syndrome wikiPageWikiLink Genetic_testing.
- Roussy–Lévy_syndrome wikiPageWikiLink Gustave_Roussy.
- Roussy–Lévy_syndrome wikiPageWikiLink Hyporeflexia.
- Roussy–Lévy_syndrome wikiPageWikiLink Kyphoscoliosis.
- Roussy–Lévy_syndrome wikiPageWikiLink Life_expectancy.
- Roussy–Lévy_syndrome wikiPageWikiLink MPZ.
- Roussy–Lévy_syndrome wikiPageWikiLink Missense_mutation.
- Roussy–Lévy_syndrome wikiPageWikiLink Muscle_atrophy.
- Roussy–Lévy_syndrome wikiPageWikiLink Mutation.
- Roussy–Lévy_syndrome wikiPageWikiLink Myelin.
- Roussy–Lévy_syndrome wikiPageWikiLink Myelin_protein_zero.
- Roussy–Lévy_syndrome wikiPageWikiLink Myelin_sheath.
- Roussy–Lévy_syndrome wikiPageWikiLink Nerve.
- Roussy–Lévy_syndrome wikiPageWikiLink Nerve_biopsy.
- Roussy–Lévy_syndrome wikiPageWikiLink Nerve_conduction_velocity.
- Roussy–Lévy_syndrome wikiPageWikiLink Nerve_damage.
- Roussy–Lévy_syndrome wikiPageWikiLink Nerve_injury.
- Roussy–Lévy_syndrome wikiPageWikiLink Neuron.
- Roussy–Lévy_syndrome wikiPageWikiLink Neurons.
- Roussy–Lévy_syndrome wikiPageWikiLink PMP22.
- Roussy–Lévy_syndrome wikiPageWikiLink Palliative_care.
- Roussy–Lévy_syndrome wikiPageWikiLink Peripheral_myelin_protein_22.
- Roussy–Lévy_syndrome wikiPageWikiLink Peroneus.
- Roussy–Lévy_syndrome wikiPageWikiLink Peroneus_muscles.
- Roussy–Lévy_syndrome wikiPageWikiLink Pes_cavus.
- Roussy–Lévy_syndrome wikiPageWikiLink Physical_therapy.
- Roussy–Lévy_syndrome wikiPageWikiLink Protein.
- Roussy–Lévy_syndrome wikiPageWikiLink Reflex.
- Roussy–Lévy_syndrome wikiPageWikiLink Schwann_cell.
- Roussy–Lévy_syndrome wikiPageWikiLink Schwann_cells.
- Roussy–Lévy_syndrome wikiPageWikiLink Sensory_loss.
- Roussy–Lévy_syndrome wikiPageWikiLink Surgery.
- Roussy–Lévy_syndrome wikiPageWikiLink Water_cure_(therapy).
- Roussy–Lévy_syndrome wikiPageWikiLink Water_therapy.
- Roussy–Lévy_syndrome wikiPageWikiLinkText "Roussy–Lévy syndrome".
- Roussy–Lévy_syndrome hasPhotoCollection Roussy–Lévy_syndrome.
- Roussy–Lévy_syndrome icd "334.3".
- Roussy–Lévy_syndrome icd "G60.0".
- Roussy–Lévy_syndrome name "Roussy–Lévy syndrome".
- Roussy–Lévy_syndrome omim "180800".
- Roussy–Lévy_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Roussy–Lévy_syndrome wikiPageUsesTemplate Template:Reflist.
- Roussy–Lévy_syndrome subject Category:Autosomal_dominant_disorders.
- Roussy–Lévy_syndrome subject Category:Neurogenetic_disorders.
- Roussy–Lévy_syndrome type Disease.
- Roussy–Lévy_syndrome type Thing.
- Roussy–Lévy_syndrome type Q12136.
- Roussy–Lévy_syndrome comment "Roussy–Lévy syndrome, also known as Roussy–Lévy hereditary areflexic dystasia, is a rare genetic disorder of humans that results in progressive muscle wasting. It is caused by mutations in the genes that code for proteins necessary for the functioning of the myelin sheath of the neurons, affecting the conductance of nerve signals and resulting in loss of muscles' ability to move.The condition affects people from infants through adults and is inherited in an autosomal dominant manner.".
- Roussy–Lévy_syndrome label "Roussy–Lévy syndrome".
- Roussy–Lévy_syndrome sameAs m.0k2kf29.
- Roussy–Lévy_syndrome sameAs Q7371349.
- Roussy–Lévy_syndrome sameAs Q7371349.
- Roussy–Lévy_syndrome wasDerivedFrom Roussy–Lévy_syndrome?oldid=678481085.
- Roussy–Lévy_syndrome isPrimaryTopicOf Roussy–Lévy_syndrome.
- Roussy–Lévy_syndrome name "Roussy–Lévy syndrome".