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Journal of Clinical Immunology

, Volume 34, Issue 5, pp 521–523 | Cite as

A Novel Splice Site Mutation in the SERPING1 Gene Leads to Haploinsufficiency by Complete Degradation of the Mutant Allele mRNA in a Case of Familial Hereditary Angioedema

  • Roger Colobran
  • Ricardo Pujol-BorrellEmail author
  • Manuel Hernández-González
  • Mar Guilarte
Letter to Editor

Abstract

Hereditary angioedema due to C1-inhibitor deficiency (HAE-C1INH) is a rare autosomal-dominant and life-threatening disorder caused by mutations in SERPING1 gene. It is characterized by attacks of angioedema involving the skin and/or the mucosa of the upper airways, as well as the intestinal mucosa. Here we report the case of a patient with HAE-C1INH without family history of angioedema. By sequencing the SERPING1 gene we detected a novel mutation (c.1249 + 5G > A) affecting the 5’ donor splice site in intron 7. We analyzed the SERPING1 cDNA expecting a defect in splicing process but only the wild type allele was detected. SNP analysis of the cDNA sequence demonstrated that only one of the two alleles was present, indicating that the mRNA from the mutated allele was completely degraded. This study reinforces the concept of incomplete penetrance of this disorder since the patients’ mother never presented any sign of angioedema despite carrying the same mutation.

Keywords

Angioedema Splice Site Mutation Donor Splice Site Hereditary Angioedema Splice Process 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer Science+Business Media New York 2014

Authors and Affiliations

  • Roger Colobran
    • 1
    • 2
  • Ricardo Pujol-Borrell
    • 1
    • 4
    Email author
  • Manuel Hernández-González
    • 1
  • Mar Guilarte
    • 3
  1. 1.Immunology Division, Vall d’Hebron Research Institute (VHIR)Hospital Universitari Vall d’Hebron (HUVH)BarcelonSpain
  2. 2.Clinical and Molecular Genetic Division, Vall d’Hebron Research Institute (VHIR)Hospital Universitari Vall d’Hebron (HUVH)BarcelonSpain
  3. 3.Allergy Unit, Internal Medicine Department, Vall d’Hebron Research Institute (VHIR)Hospital Universitari Vall d’Hebron (HUVH)BarcelonSpain
  4. 4.Immunology Division, Edifici Microbiologia 4ª planta, direcció de laboratorisHospital Universitari Vall d’HebronBarcelonSpain

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