Novel SERPING1 Genetic Variant in Two Family Members with Hereditary Angioedema

Hereditary angioedema is a rare, autosomal dominant, genetic disorder characterized by recurrent episodes of angioedema. Over 800 SERPING1 gene variants have been reported, and their clinical profiles and causal genetic variants are highly heterogeneous. We report two cases of hereditary angioedema (HAE) in a Portuguese family: a 27-year-old male, under lanadelumab, and his 57-year-old father, kept on on-demand treatment. Genetic testing was performed following international guidelines. The Hereditary Angioedema Database Annotation highlighted a heterozygous insertion at exon 3 (c.336_337insC). This variant predicts a frameshift of the transcript, with the introduction of a premature STOP codon in C1-INH protein (p.Ser113LeufsTer20). We report the identification of a novel pathogenic SERPING1 variant in a family with HAE type 1, assisted by the Hereditary Angioedema Database Annotation variant prioritization tool. Our results may contribute to the identification of additional families with the same variant and can further enhance the knowledge about this condition.

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Publication Details

Journal
Acta Médica Portuguesa
Published
2026-02-09
DOI
https://doi.org/10.20344/amp.24214
Primary Topic
Coagulation, Bradykinin, Polyphosphates, and Angioedema
Type
article
Field-Weighted Citation Impact
0.00

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article

Novel SERPING1 Genetic Variant in Two Family Members with Hereditary Angioedema

Sofia Cosme Ferreira, Carlos Flores, Alexandra Rosa, Rita Câmara et al.
Acta Médica Portuguesa
Coagulation, Bradykinin, Polyphosphates, and Angioedema
article

Novel SERPING1 Genetic Variant in Two Family Members with Hereditary Angioedema

Sofia Cosme Ferreira, Carlos Flores, Alexandra Rosa, Rita Câmara, Filipa Sousa, Ariel Callero, Alejandro Mendoza-Alvarez, Rafaela González-Montelongo
article en

Abstract

Hereditary angioedema is a rare, autosomal dominant, genetic disorder characterized by recurrent episodes of angioedema. Over 800 SERPING1 gene variants have been reported, and their clinical profiles and causal genetic variants are highly heterogeneous. We report two cases of hereditary angioedema (HAE) in a Portuguese family: a 27-year-old male, under lanadelumab, and his 57-year-old father, kept on on-demand treatment. Genetic testing was performed following international guidelines. The Hereditary Angioedema Database Annotation highlighted a heterozygous insertion at exon 3 (c.336_337insC). This variant predicts a frameshift of the transcript, with the introduction of a premature STOP codon in C1-INH protein (p.Ser113LeufsTer20). We report the identification of a novel pathogenic SERPING1 variant in a family with HAE type 1, assisted by the Hereditary Angioedema Database Annotation variant prioritization tool. Our results may contribute to the identification of additional families with the same variant and can further enhance the knowledge about this condition.

Acta Médica Portuguesa
Hospital Universitario Nuestra Señora de Candelaria (ES), Agencia Regional da Energia e Ambiente da Regiao Autonoma da Madeira (PT), Instituto Tecnológico y de Energías Renovables (ES), Fundación Canaria de Investigación Sanitaria (ES), Universidade da Madeira (PT)
Ministerio de Ciencia e Innovación, Agencia Estatal de Investigación
Openalex Percentile: Top 62%
Coagulation, Bradykinin, Polyphosphates, and Angioedema
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Novel SERPING1 Genetic Variant in Two Family Members with Hereditary Angioedema — Sofia Cosme Ferreira, Carlos Flores, et al. · Acta Médica Portuguesa (2026) | TGRS Research Map | TGRS