From: Abnormal biochemical indicators of neonatal inherited metabolic disease in carriers
Case | Carriers | Non-carriers | P | |
---|---|---|---|---|
Congenital hypothyroidism | ||||
false-positive | 2 | 0 | 2 | — |
negative | 686 | 58 | 628 | |
Organic acid metabolic disease | ||||
false-positive | 99 | 12 (12.12%) | 87(87.87%) | 0.096 |
negative | 686 | 50 (7.29%) | 636(92.71%) | |
Amino acid metabolic disease | ||||
false-positive | 58 | 9 (15.52%) | 49(84.48%) | 0.030 |
negative | 686 | 46 (6.71%) | 640(93.29%) | |
Fatty acid β oxidation disorder | ||||
false-positive | 53 | 15 (28.30%) | 38(71.70%) | < 0.001 |
negative | 686 | 50 (7.29%) | 636(92.71%) |