%0 Journal Article
%T Diagnosis of cystic fibrosis: a high heterogeneity of symptoms and genotypes in a Brazil population.
%A Meneses DG
%A Dos Santos FR
%A Botelho AJ
%A Bispo LM
%A Matos CG
%A Propheta VGS
%A Rodrigues AF
%A Oliveira GU
%A da Silva AM
%A Gurgel RQ
%J BMC Pediatr
%V 24
%N 1
%D 2024 Jul 1
%M 38956483
%F 2.567
%R 10.1186/s12887-024-04891-z
%X <B>BACKGROUND: </B>In highly multiracial populations with inadequate newborn screening, knowledge of the various phenotypic presentations of Cystic Fibrosis (CF) can help reach an early diagnosis. This study aims to describe phenotypes and genotypes at the time of CF diagnosis in a state in the Northeast Region of Brazil.<BR><B>METHODS: </B>Retrospective cross-sectional study. Clinical data were extracted from the medical records of CF patients. Clinical, laboratory, and genotypic characteristics were described for patients admitted to a tertiary referral center between 2007 and 2021.<BR><B>RESULTS: </B>Fifty-eight (58) patients were included in the study, 53.5% of whom were diagnosed through clinical suspicion. The median age at diagnosis was 4.7 months (IQR: 1.5-14.8 months). Five patients had false-negative results in the newborn screening. Faltering growth was the most frequent clinical manifestation. Bronchiectasis and a history of pneumonia predominated in those older than ten, while thinness, underweight, and electrolyte imbalances were more frequent in children under two. Sequencing of the CFTR gene identified 27 genotypes, with at least one class I-III variant in all patients, and nine variants that are rare, previously undescribed, or have uncertain significance (619delA, T12991, K162Q, 3195del6, 1678del > T, 124del123bp, 3121-3113 A > T). The most frequent alleles were p.Phe508del, p.Gly542*, p.Arg334Trp, and p.Ser549Arg.<BR><B>CONCLUSIONS: </B>Malnutrition and electrolyte imbalances were the most frequent phenotypes for children < 2 years and were associated with genotypes including 2 class I-III variants. Rare and previously undescribed variants were identified. The p.Gly542*, p.Arg334Trp, and p.Ser549Arg alleles were among the most frequent variants in this population.