Emerging Insights into Hereditary Alpha-Tryptasemia in the Context of Mast Cell Disorders: A Greek Case Series

genotyping may provide additional genetic information that aids in contextualizing clinical heterogeneity and mediator-related symptom burden in patients with mast cell disorders. Incorporation of HαT testing into routine evaluation may optimize individualized management.

Authors

Sotirios G. Papageorgiou (ORCID: https://orcid.org/0000-0002-3376-837X)
Niki Papapostolou (ORCID: https://orcid.org/0000-0003-3950-3089)
Maria Martinou
A. Bouchla
Styliani Taka
Natalia Katrachoura
Michael Makris
Fotios Koliofotis

Institutions

National and Kapodistrian University of Athens (GR)
University General Hospital Attikon (GR)

Publication Details

Journal: Journal of Personalized Medicine
Published: 2026-04-01
DOI: https://doi.org/10.3390/jpm16040196
Primary Topic: Mast cells and histamine
Type: article
Field-Weighted Citation Impact: 0.00

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article

Emerging Insights into Hereditary Alpha-Tryptasemia in the Context of Mast Cell Disorders: A Greek Case Series

Sotirios G. Papageorgiou, Niki Papapostolou, Maria Martinou, A. Bouchla et al.

Apr 1, 2026

Journal of Personalized Medicine

Mast cells and histamine

article

Emerging Insights into Hereditary Alpha-Tryptasemia in the Context of Mast Cell Disorders: A Greek Case Series

Sotirios G. Papageorgiou, Niki Papapostolou, Maria Martinou, A. Bouchla, Styliani Taka, Natalia Katrachoura, Michael Makris, Fotios Koliofotis

April 1, 2026article en

Abstract

Journal of Personalized MedicineVol. 16(4)

National and Kapodistrian University of Athens (GR), University General Hospital Attikon (GR)

Good health and well-being

Openalex Percentile: Top 31%

Mast cells and histamine

DOI Open Access PDF OpenAlex

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Emerging Insights into Hereditary Alpha-Tryptasemia in the Context of Mast Cell Disorders: A Greek Case Series — Sotirios G. Papageorgiou, Niki Papapostolou, et al. · Journal of Personalized Medicine (2026) | TGRS Research Map | TGRS