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Table 3 Clinical features of patients with epilepsy and with m.15218A > G

From: Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus

Patient ID

Sex

Age at onset

Seizure classification

Etiology

Family history

37

F

7

Generalized tonic-clonic seizures

Unknown

Sister with epilepsy

75

F

47

Focal with impairment of consciousness, involving subjective sensory phenomena, evolving to a bilateral, convulsive seizure

Unknown

Sister with epilepsy

43

F

0.5

Focal with impairment of consciousness, with observable motor or autonomic components, occasionally evolving to a bilateral, convulsive seizure

Unknown

Mother, brother with epilepsy

52

F

62

Focal with impairment of consciousness and with observable motor components

Structural

Brother, sister with DM, sister with HI

53

M

25

Focal with impairment of consciousness, involving subjective sensory phenomena

Unknown

Mother with HI

  1. DM diabetes mellitus, HI hearing impairment. Seizure classification and assessment of etiology conform to the criteria in the Report of the ILAE Commission on Classification and Terminology [40].