PedAM
Pediatric Disease Annotations & Medicines
| Disease | hemiplegic migraine |
| Phenotype | C0149931|migraine |
| Sentences | 8 |
| 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- 22319646 | Few studies have investigated headache subtype, but migraines and mimics of hemiplegic migraine seem to be more prevalent [27, 40]. |
| PubMedID- 21457239 | Calcitonin gene-related peptide does not cause migraine attacks in patients with familial hemiplegic migraine. |
| 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. |
| PubMedID- 22027350 | In this review, we consider the emerging genetic discoveries about migraine, beginning with familial hemiplegic migraine, where the search for causative genes has been particularly rewarding. |
| 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- 24898624 | Background: cacna1a gene disorders present a variable familial phenotype of ataxia, migraine with aura, and/or hemiplegic migraine. |
| PubMedID- 23918834 | Case: here we report on a three-generation family with five patients having a novel atp1a2 mutation on exon 19, causing guanine-to-adenine substitution (c.2620g>a, p.gly874ser) that co-segregated in the five living relatives with migraine, four of whom had hemiplegic migraine. |
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