PedAM
Pediatric Disease Annotations & Medicines
| Disease | ataxia |
| Phenotype | C0149931|migraine |
| Sentences | 3 |
| PubMedID- 22527033 | We report a 54-year-old woman, among the population of the lombardia gens project (http://www.clinicaltrial.gov), affected by migraine with aura and ataxia carrying the p.arg583gln missense substitution in the cacna1a gene focusing, through a review literature, on the clinical phenotype of mutation carriers. |
| PubMedID- 24898624 | Objective: the aim of this study is to report a minimal prevalence estimate for familial hemiplegic migraine with cerebellar ataxia and spinocerebellar ataxia type 6 in portugal. |
| PubMedID- 24101904 | Furthermore, we found that 4 additional patients carrying homozygous nbce1 mutations had the following types of migraine: hemiplegic migraine with episodic ataxia in the patient with l522p (demirci et al., 2006), migraine with aura in the patient with n721tfsx29 (inatomi et al., 2004), and migraine without aura in the patients with r510h and r881c (igarashi et al., 1999; horita et al., 2005). |
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