| Literature DB >> 27117206 |
Anne Bergougnoux1, Amandine Boureau-Wirth2, Cécile Rouzier2, Jean-Pierre Altieri3, Fanny Verneau3, Lise Larrieu3, Michel Koenig4, Mireille Claustres4, Caroline Raynal4.
Abstract
The detection of two frequent CFTR disease-causing variations in the context of a newborn screening program (NBS) usually leads to the diagnosis of cystic fibrosis (CF) and a relevant genetic counseling in the family. In the present study, CF-causing variants p.Phe508del (F508del) and c.3140-26A>G (3272-26A>G) were identified on a neonate with positive ImmunoReactive Trypsinogen test by the Elucigene™ CF30 kit. The CF diagnosis initially suggested, despite three inconclusive Sweat Chloride Tests (SCT), was finally ruled out after the familial segregation study combined with a negative SCT. Haplotype studies, based on the comparison of 80 p.Phe508del haplotypes, suggested a probable de novo occurrence of c.3140-26A>G on the p.Phe508del ancestral allele in this family. This false positive case emphasizes the importance of SCT in the NBS strategy. Moreover, it raises the need for familial segregation studies in CF and in overall molecular diagnosis strategy of autosomal recessive diseases.Entities:
Keywords: CFTR gene; Complex allele; Cystic fibrosis; False positive; Newborn screening
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Year: 2016 PMID: 27117206 DOI: 10.1016/j.jcf.2016.04.003
Source DB: PubMed Journal: J Cyst Fibros ISSN: 1569-1993 Impact factor: 5.482