MCID: HMP020
MIFTS: 1

Hemiplegia Alterans

Aliases & Classifications for Hemiplegia Alterans

MalaCards integrated aliases for Hemiplegia Alterans:

Name: Hemiplegia Alterans 51

Summaries for Hemiplegia Alterans

NINDS : 51 Alternating hemiplegia is a rare neurological disorder that develops in childhood, most often before the child is 18 months old. The disorder is characterized by recurrent episodes of paralysis that involve one or both sides of the body, multiple limbs, or a single limb. The paralysis may affect different parts of the body at different times and may be brief or last for several days. Oftentimes these episodes will resolve after sleep. Affected children may also have abnormal movements involving stiffening or "dance-like" movements of a limb, as well as walking and balance problems. Some children have seizures. Children may have normal or delayed development. There are both benign and more serious forms of the disorder. Most children do not have a family history of the disorder; however, recent studies have show that some children with a family history have mutations in the genes CACNA1A, SCN1A, and ATP1A2. Mutations in the ATP1A2 gene have previously been associated with families affect by familial hemiplegic migraine.

MalaCards based summary : Hemiplegia Alterans

Related Diseases for Hemiplegia Alterans

Symptoms & Phenotypes for Hemiplegia Alterans

Drugs & Therapeutics for Hemiplegia Alterans

Search Clinical Trials , NIH Clinical Center for Hemiplegia Alterans

Genetic Tests for Hemiplegia Alterans

Anatomical Context for Hemiplegia Alterans

Publications for Hemiplegia Alterans

Variations for Hemiplegia Alterans

Expression for Hemiplegia Alterans

Search GEO for disease gene expression data for Hemiplegia Alterans.

Pathways for Hemiplegia Alterans

GO Terms for Hemiplegia Alterans

Sources for Hemiplegia Alterans

3 CDC
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10 dbSNP
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16 ExPASy
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65 SNOMED-CT via HPO
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70 UMLS via Orphanet
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