Abstract
Background and aim: Cystic Fibrosis (CF) is a monogenic disorder with heterogeneous phenotypic presentation. In atypical cases, the sweat test may show border-line or normal values and the diagnosis involves the search for mutations in the CFTR gene, clinical features and follow-up.
Case report: We present a case of an adolescent boy affected by recurrent acute pancreatitis (AP) started at puberty, with normal sweat values, carrier of compound heterozygosity (I507del+IVS8(5T)). The I507del mutation is a severe CFTR mutation. In contrast, the IVS8(5T) mutation is not associated with clinical cystic fibrosis but, in compound heterozigosity with a more severe mutation, can be causative of mono- or oligo-symptomatic CFTR-related disorders.
Conclusion: This is probably the first case report of an atypical CF in a patient with the compound heterozygosity I507del+IVS8 5T. It confirms the challenges and difficulties for diagnosing atypical CF and highlights the role of CFTR mutations in the pathogenesis of idiopathic pancreatitis.
Details
| Primary Language | English |
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| Authors | |
| Publication Date | November 30, 2010 |
| DOI | https://doi.org/10.17334/jps.35271 |
| IZ | https://izlik.org/JA25FW27LU |
| Published in Issue | Year 2010 Volume: 2 Issue: 6 |