eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | familial hemiplegic migraine |
| Comorbidity | C0149931|migraine |
| Sentences | 5 |
| PubMedID- 20301562 | In migraine with aura (including familial hemiplegic migraine) the neurologic symptoms of aura are unequivocally localizable to the cerebral cortex or brain stem and include visual disturbance (most common), sensory loss (e.g., numbness or paresthesias of the face or an extremity), and dysphasia (difficulty with speech); fhm must include motor involvement, i.e., hemiparesis (weakness of an extremity). |
| PubMedID- 21784774 | Objective: the aim was to identify and describe migraine trigger factors in patients with familial hemiplegic migraine (fhm) from a population-based sample. |
| PubMedID- 21457239 | Calcitonin gene-related peptide does not cause migraine attacks in patients with familial hemiplegic migraine. |
| PubMedID- 23165010 | Missense mutations in cacna1a, the gene that encodes the pore-forming alpha1 subunit of human voltage-gated ca(v)2.1 (p/q-type) calcium channels, cause a rare form of migraine with aura (familial hemiplegic migraine type 1: fhm1). |
| PubMedID- 20194127 | A subtype of migraine with aura (familial hemiplegic migraine type 1: fhm1) is caused by mutations in cav2.1 (p/q-type) ca2+ channels. |
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