Dehydrated patient without clinically evident cause: A case report

Figure 1 Molecular diagnosis showed the following heterozygous mutations: G126D and F508del in the gene CFTR. A: Locus of cystic fibrosis transmembrane conductance regulator gene on Chromosome 7q31.2. The figure was created and modified by DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans using Ensembi Resources; B: Graphic view of cystic fibrosis transmembrane conductance regulator with pathogenic variants of our patient.