Johanson-Blizzard Syndrome: Expanding the Phenotype of Exocrine Pancreatic Insufficiency

  • Kate M Ellery Division of Gastroenterology, Hepatology, and Nutrition, Nationwide Children’s Hospital, The Ohio State University College of Medicine, Columbus, Ohio, USA
  • Steven H Erdman Division of Gastroenterology, Hepatology, and Nutrition, Nationwide Children’s Hospital, The Ohio State University College of Medicine, Columbus, Ohio, USA
Keywords: Ectodermal Dysplasia, Exocrine Pancreatic Insufficiency, Johanson Blizzard syndrome

Abstract

Context Johanson-Blizzard syndrome (JBS) is a rare autosomal recessive syndrome characterized by dysmorphic nasal alae, ectodermal abnormalities, exocrine pancreatic insufficiency and early growth failure. Most patients are diagnosed by clinical criteria prenatally or in early infancy. Nonsense, frame shift and splice-site mutations of the ubiquitin ligase gene (UBR1) lead to early loss of acinar cells in individuals with JBS. Case report We describe a previously asymptomatic patient with ectodermal dysplasia presenting with sudden onset exocrine pancreatic insufficiency in adolescence. The family reports an identical twin brother with similar symptoms. Conclusion This case illustrates that the phenotypic variability of pancreatic involvement in JBS may be subtle and may not manifest until the second decade of life. We suspect that this mild phenotype results from mutations in UBR1 allowing for partial function.

Image. Thick yellow toe nails consistent with ectodermal dysplasia.

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References

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Thick yellow toe nails consistent with ectodermal dysplasia
Published
2014-07-28
How to Cite
ElleryK., & ErdmanS. (2014). Johanson-Blizzard Syndrome: Expanding the Phenotype of Exocrine Pancreatic Insufficiency. JOP. Journal of the Pancreas, 15(4), 388-390. https://doi.org/10.6092/1590-8577/2409
Section
CASE REPORTS