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Table 1 Demographic characteristics of 103 NMD patients

From: Reliability and validity of the Thai pediatric quality of life inventory™ 3.0 neuromuscular module

Data

Median ± IQR (range) or n (%)

Age of onset (years)

4 ± 5 (0–11)

Age at time of the evaluation (years)

11 ± 7 (2–18)

2–4

7 (6.8)

5–7

19 (18.4)

8–12

38 (36.9)

13–18

39 (37.9)

Male

78 (75.7)

Diagnosis

 Duchenne Muscular Dystrophy (DMD)

57 (55.3)

 Charcot-Marie-Tooth (CMT)

10 (9.7)

 Spinal Muscular Atrophy (SMA)

8 (7.8)

 Other

28 (27.2)

 Non-ambulatory patients

49 (47.6)

 Positive Family History

29 (28.2)

 Currently in school

52 (50.5)