J Pediatr Genet 2022; 11(03): 232-235
DOI: 10.1055/s-0040-1717109
Case Report

Chronic pancreatitis caused by a Homozygous SPINK1 c.194 + 2T > C variant and Pancreas Divisum in a 3-year-old child—case report

Authors

  • Katarzyna Zdanowicz

    1   Department of Pediatrics, Gastroenterology, Hepatology, Nutrition and Allergology, Medical University of Bialystok, Bialystok, Poland
  • Miroslawa Uscinowicz

    1   Department of Pediatrics, Gastroenterology, Hepatology, Nutrition and Allergology, Medical University of Bialystok, Bialystok, Poland
  • Magdalena Rakowska

    2   Department of Gastroenterology, Hepatology, Feeding Disorders and Pediatrics, Children's Memorial Health Institute, Warsaw, Poland
  • Katarzyna Wertheim-Tysarowska

    3   Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland
  • Agnieszka Magdalena Rygiel

    3   Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland
  • Grzegorz Oracz

    2   Department of Gastroenterology, Hepatology, Feeding Disorders and Pediatrics, Children's Memorial Health Institute, Warsaw, Poland
  • Dariusz Marek Lebensztejn

    1   Department of Pediatrics, Gastroenterology, Hepatology, Nutrition and Allergology, Medical University of Bialystok, Bialystok, Poland

Funding None.
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Abstract

Chronic pancreatitis (CP) is a rare disease in children. We describe the first case of a 3-year-old Caucasian patient with CP with the presence of a homozygous pathogenic variant c.194 + 2T > C in serine protease inhibitor, Kazal type 1 (SPINK1) and pancreas divisum.



Publication History

Received: 14 July 2020

Accepted: 21 August 2020

Article published online:
05 October 2020

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