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. Author manuscript; available in PMC: 2023 Aug 14.
Published in final edited form as: Arch Neurol. 2009 Jan;66(1):85–91. doi: 10.1001/archneurol.2008.526

Table 1.

Proportion of Subjects by Group Who Responded Affirmatively to a Structured Medical History Questionnaire

Percentage (Mean [SD])
Symptom Patients With MELAS Carrier Relatives Controls P Valuea

Headache 91 58 52 <.001b,c
Balance difficulty 81 20   4 <.001b,c
Age at onset of migraines, y 77 (19.3 [10.0]) 32 (21.9 [12.3]) 16 (21.3 [10.4]) <.001b,d
Limb weakness 71 22   4 <.001b,c,d
Age at onset of clumsiness, y 62 (19 [14]) 23 (37 [17])   4 <.001b,c,d
Age at onset of myoclonus, y 50 (24 [17]) 15 (33 [15])   0 <.001b,c,d
Loss of sensation 48 19   4 <.001b,d

Abbreviation: MELAS, mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (syndrome).

a

The χ2 test was used to evaluate the heterogeneity across the 3 groups.

b

Significant difference between patients and carrier relatives.

c

Significant difference between carrier relatives and controls.

d

Significant difference between patients and controls.