Elevated tryptase level in a child with idiopathic anaphylaxis: a case of hereditary alpha-tryptasemia
- PMID: 38539267
- PMCID: PMC10976751
- DOI: 10.1186/s13223-023-00858-4
Elevated tryptase level in a child with idiopathic anaphylaxis: a case of hereditary alpha-tryptasemia
Abstract
Hereditary alpha-tryptasemia (HαT) is an autosomal dominant disorder estimated to affect 5% of the population. High baseline tryptase level is a consistent finding, but there is a great variability of clinic manifestations, including no symptoms at all. We describe a case of HαT in a 5 years 8 months old girl manifesting with idiopathic anaphylaxis and elevated baseline tryptase level. As more cases of HαT are described, a better understanding of the clinical phenotype will be acquired.
Keywords: Elevated tryptase level; Hereditary alpha-tryptasemia; Idiopathic anaphylaxis.
© 2024. Crown.
Conflict of interest statement
The authors declare that they have no competing interests.
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