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. Author manuscript; available in PMC: 2019 Jul 1.
Published in final edited form as: J Child Neurol. 2018 May 15;33(8):537–545. doi: 10.1177/0883073818773029

Table 2.

Median age (years) and interquartile range (IQR) at various diagnostic steps for term and preterm males with Duchenne muscular dystrophy and no family history of dystrophinopathy at birth, MD STARnet

Preterm births Term births P value*
N Median age (IQR) N Median age (IQR)
Earliest mobility signs/symptoms 30 2.00 (2.16) 294 2.01 (2.67) 0.84
Initial medical evaluation 30 2.59 (2.83) 293 4.01 (3.08) 0.07
First neuromuscular visit 30 4.25 (2.80) 295 5.00 (3.00) 0.23
First abnormal CK test 25 4.17 (2.42) 275 4.92 (3.08) 0.19
DNA test 29 4.87 (3.28) 276 5.65 (3.47) 0.23
Muscle biopsy test 12 3.79 (1.99) 136 5.23 (3.24) 0.18
Definitive diagnosis** 30 4.25 (3.42) 295 4.92 (3.00) 0.26
*

Wilcoxon rank-sum test; IQR = interquartile range; MD STARnet = Muscular Dystrophy Surveillance Tracking and Research Network;

CK = creatine kinase

**

We determined the age at definitive diagnosis to be the minimum value among the age at first abnormal CK, age at MB and age at DNA test