Literature DB >> 24653987

Can a polymorphism in the thalassemia gene and a heterozygote CFTR mutation cause acute pancreatitis?

J-Matthias Löhr1, Stephan Haas1.   

Abstract

The case of a 32-year-old black woman of African descent who suffered from repeated episodes of acute pancreatitis, initially triggered when flying on airplanes, is reported. She did not drink alcohol or smoke. Genetic analysis was negative for cationic trypsinogen, serine protease inhibitor Kazal type 1 and chymotrypsin C. However, hemoglobin F was elevated. Sequencing of the thalassemia gene revealed a novel alteration in the 5' region indicative of a functional abnormality of the molecule. Sequencing the cystic fibrosis transmembrane conductance regulator (CFTR) gene revealed a heterozygote sequence variant. The combination of a hemoglobin gene mutation known for thalassemia in conjunction with the hitherto undescribed CFTR mutation is suggested to pave the road for initial and repetitive pancreatitis attacks. This will be discussed.

Entities:  

Keywords:  Acute pancreatitis; Cystic fibrosis transmembrane conductance regulator; Flying; Hemoglobin; Hereditary persistence of fetal hemoglobin; Hypoxia; Thalassemia

Year:  2014        PMID: 24653987      PMCID: PMC3955802          DOI: 10.12998/wjcc.v2.i3.62

Source DB:  PubMed          Journal:  World J Clin Cases        ISSN: 2307-8960            Impact factor:   1.337


  23 in total

1.  Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis.

Authors:  H Witt; W Luck; H C Hennies; M Classen; A Kage; U Lass; O Landt; M Becker
Journal:  Nat Genet       Date:  2000-06       Impact factor: 38.330

2.  Detection of haemoglobin variants and inference of their functional properties using complete oxygen dissociation curve measurements.

Authors:  K Imai; P Tientadakul; N Opartkiattikul; P Luenee; P Winichagoon; J Svasti; S Fucharoen
Journal:  Br J Haematol       Date:  2001-02       Impact factor: 6.998

3.  Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant.

Authors:  M Losekoot; R Fodde; E J Gerritsen; I van de Kuit; A Schreuder; P C Giordano; J M Vossen; L F Bernini
Journal:  Blood       Date:  1991-02-15       Impact factor: 22.113

4.  Compound heterozygosity for a beta zero-thalassemia (frameshift codons 38/39; -C) and a nondeletional Swiss type of HPFH (A----C at NT -110, G gamma) in a Czechoslovakian family.

Authors:  K Indrak; J Indrakova; F Kutlar; D Pospisilova; I Sulovska; E Baysal; T H Huisman
Journal:  Ann Hematol       Date:  1991-08       Impact factor: 3.673

5.  Bifid tail of the pancreas: benign bifurcation anomaly.

Authors:  Dietmar Dinter; J-Matthias Löhr; K Wolfgang Neff
Journal:  AJR Am J Roentgenol       Date:  2007-11       Impact factor: 3.959

6.  Variability in the fetal hemoglobin level of the normal adult.

Authors:  E G Kazanetz; N S Smetanina; A D Adekile; G D Efremov; T H Huisman
Journal:  Am J Hematol       Date:  1996-10       Impact factor: 10.047

Review 7.  Disturbances of the microcirculation in acute pancreatitis.

Authors:  C M Cuthbertson; C Christophi
Journal:  Br J Surg       Date:  2006-05       Impact factor: 6.939

Review 8.  Ischemia/Reperfusion-Induced pancreatitis.

Authors:  G H Sakorafas; G G Tsiotos; M G Sarr
Journal:  Dig Surg       Date:  2000       Impact factor: 2.588

9.  The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs.

Authors:  E A Rachmilewitz; H Tamari; F Liff; Y Ueda; R L Nagel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 10.  Chronic pancreatitis: challenges and advances in pathogenesis, genetics, diagnosis, and therapy.

Authors:  Heiko Witt; Minoti V Apte; Volker Keim; Jeremy S Wilson
Journal:  Gastroenterology       Date:  2007-04       Impact factor: 22.682

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