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. 2023 Jul 26;39:100847. doi: 10.1016/j.lanwpc.2023.100847

Table 2.

Subject characteristics.

Parameter (unit) Statistics/category Unit (%)
Age (months) Number of subjects 23
Mean 9.0
Standard deviation 6.3
Maximum 23
Median 7.0
Minimum 2
Sex Male 12 (52.17)
Female 11 (47.83)
Height Number of subjects 23
Mean 68.82
Standard deviation 7.88
Maximum 82.3
Median 70.40
Minimum 57.1
Weight (kg) Number of subjects 23
Mean 7.611
Standard deviation 1.651
Maximum 10.21
Median 7.500
Minimum 4.91
Ethnicity Japanese 23 (100.00)
Race Asian 23 (100.00)
Primary disease: Disease group Congenital esophageal atresia 6 (26.09)
Airway stenosis 5 (21.74)
Neuromuscular disease 5 (21.74)
Inherited metabolic diseasea 4 (17.39)
Pulmonary hypoplasia 3 (13.04)
Primary disease: Disease name Congenital esophageal atresia 6 (26.09)
Propionic acidemia 2 (8.70)
Pharyngeal stenosis 2 (8.70)
Laryngomalacia 2 (8.70)
Congenital diaphragmatic hernia 2 (8.70)
Duchenne muscular dystrophy 1 (4.35)
Pharyngeal stenosis/laryngomalacia 1 (4.35)
Very long-chain acyl-coenzyme A dehydrogenase deficiency 1 (4.35)
Myotonic dystrophy 1 (4.35)
Spinal muscular atrophy 1 (4.35)
Congenital myopathy 1 (4.35)
Congenital myopathy (suspected Bethlem myopathy) 1 (4.35)
Congenital cystic lung disease 1 (4.35)
Medium-chain acyl-coenzyme A dehydrogenase deficiency 1 (4.35)
a

Propionic acidemia (2 cases), medium-chain acyl-CoA dehydrogenase (1 case), deficiency very-long-chain acyl-CoA dehydrogenase (1 case).