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Roussy-LÃ©vy syndrome

1 OMIM reference -
2 associated genes
6 signs/symptoms

PROTEIN INTERACTIONS: 1

Alternating hemiplegia of childhood

2 OMIM references -
4 associated genes
No signs/symptoms info

Roussy-LÃ©vy syndrome

Alternating hemiplegia of childhood

MPZ	(UniProt - OMIM)		ATP1A2	(UniProt - OMIM)
PMP22	(UniProt - OMIM)		ATP1A3	(UniProt - OMIM)
			CACNA1A	(UniProt - OMIM)
			SLC1A3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PMP22	(0.63)	ATP1A2

Citations in the biomedical literature:

Roussy-LÃ©vy syndrome		Alternating hemiplegia of childhood
	Synonym(s): - Hereditary areflexic dystasia, Roussy-LÃ©vy type		Synonym(s): - AHC - Alternating hemiplegia in childhood

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C536589

Roussy-LÃ©vy syndrome
	Very frequent - Abnormal gait - Areflexia / hyporeflexia - Autosomal recessive inheritance - Movement disorder - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Nerve conduction abnormality
Alternating hemiplegia of childhood
(no data available)