MCID: FML365
MIFTS: 1

Familiar or Sporadic Hemiplegic Migraine

Categories: Rare diseases

Aliases & Classifications for Familiar or Sporadic Hemiplegic Migraine

MalaCards integrated aliases for Familiar or Sporadic Hemiplegic Migraine:

Name: Familiar or Sporadic Hemiplegic Migraine 52

Classifications:



Summaries for Familiar or Sporadic Hemiplegic Migraine

NIH Rare Diseases : 52 Familial or sporadic hemiplegic migraine refers to a rare type of migraine with aura that occurs with motor weakness during the aura. The two types of hemiplegic migraine (HM) are distinguished based on the family history : familial hemiplegic migraine (FHM, in which at least one other family member has the condition) and sporadic hemiplegic migraine (SHM, in which there is no family history). Signs and symptoms vary but may include visual disturbances, sensory loss, difficulty with speech, weakness on one side of the body, confusion, and impaired consciousness. Severe attacks may occur in both types with prolonged hemiplegia, coma, fever and/or seizures . FHM may be caused by a mutation in any of several genes and is inherited in an autosomal dominant manner.

MalaCards based summary : Familiar or Sporadic Hemiplegic Migraine

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Sources for Familiar or Sporadic Hemiplegic Migraine

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
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30 HMDB
31 HPO
32 ICD10
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68 SNOMED-CT via HPO
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