1.
J Pediatr
; 153(6): 857-9, 2008 Dec.
Article
in English
| MEDLINE
| ID: mdl-19014821
ABSTRACT
The reference ranges for sweat [C1(-)] were reevaluated in 300 infants referred to our Center as carriers of at least 1 cystic fibrosis mutation identified through newborn screening. The recommended borderline range of 30 to 59 mmol/L failed to identify all individuals who were compound heterozygotes. Our data support using a borderline range of 24 to 59 mmol/L.