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PedAM

Pediatric Disease Annotations & Medicines




Disease epilepsy
Symptom C0149931|migraine
Sentences 13
PubMedID- 20112041 The prevalence of migraine in children with partial epilepsy was 21% in benign rolandic epilepsy and 17% in cryptogenic/symptomatic epilepsy 7.
PubMedID- 21437711 A headache attack with migraine phenotype in patients with epilepsy thus might be associated with otherwise clinically silent seizures, calling into question the rigid differentiation between interictal and ictal headache.
PubMedID- 24063537 In fact, it has been found an increased risk of migraine in people with epilepsy caused by head trauma, and that in each subgroup of epilepsy, defined on the basis of seizure type, age at onset, etiology, and family history .
PubMedID- 25216447 Results: maternal epilepsy treated with carbamazepine and migraine were found to be associated with higher risk of ventricular septal defect; panic disorders were associated with higher risk of hypoplastic left heart; type i diabetes mellitus was associated with higher risk of coarctation of the aorta; chronic hypertension was associated with higher risk of ventricular septal defect, common atrioventricular canal and common truncus; and paroxysmal supraventricular tachycardia was associated with higher risk of atrial septal defect secundum, common atrioventricular canal and ventricular septal defect.
PubMedID- 24400104 In the past three decades, the clinical relevance of csd attracted lots of attention, and csd was considered to be involved in migraine with aura, epilepsy and ischemic stroke .
PubMedID- 24296772 Studies indicate a definite association of epilepsy with migraine headaches and a significant number of migraneurs are found to be epileptic.
PubMedID- 25362099 The comorbidity-specific ahr for developing epilepsy associated with migraine was 2.33 (95% ci = 1.25-4.34) in patients without any comorbidities, and 1.73 (95% ci = 1.02-2.93) in those with comorbidities.
PubMedID- 20191013 migraine prevalence in patients with epilepsy ranged from 8% to 15%.
PubMedID- 22217520 Description: an individual can suffer both from headaches (either migraine and/or other type of headache) and epilepsy, either by chance or because of a common underlying pathology.
PubMedID- 20963464 Moreover, up to 75% of fhm families have a mutation in the p/q-type calcium channel ca(v)2.1 subunit cacna1a gene on chromosome 19p13, while a candidate region of 9.95 cm (5.96 mb) between markers gata152h04 and d9s253 located at chromosome 9q21–q22 was identified in a large belgian family with occipitotemporal lobe epilepsy associated with migraine with visual aura .
PubMedID- 23306109 In paps, epilepsy correlated with ss2gpi-igm, migraine with acl-igm, and thrombocytopenia with acl-igm, acl-igg, anti ss2gpi-igg and la.
PubMedID- 21188255 A linkage analysis in a large belgian family with occipitotemporal lobe epilepsy associated with migraine with visual aura provided evidence for a novel epilepsy and migraine susceptibility locus on chromosome 9q21–q22 (deprez et al., 2007).
PubMedID- 24045571 Background: sturge-weber syndrome (sws) is an uncommon etiology of hemiplegic migraine-like (hm-like) attacks, associated with epilepsy and mental retardation.

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