Gender equity in hemophilia: need for healthcare, familial, and societal advocacy
- PMID: 38646558
- PMCID: PMC11026857
- DOI: 10.3389/fmed.2024.1345496
Gender equity in hemophilia: need for healthcare, familial, and societal advocacy
Abstract
Hemophilia is a rare bleeding disorder caused by a genetic defect on chromosome X. It is inherited as an X-linked trait, and hence, it is more frequently diagnosed in males, whereas women have been traditionally considered only as carriers of the disease. However, the role of women in families of patients with hemophilia is pivotal. As mothers, sisters, daughters, and female partners of patients with hemophilia, they play a central role in the management of the patient, considering healthcare, social, and familial aspects, but they might be affected by the disease as well, particularly in regions where consanguinity is frequent. This paper aims to explore the involvement of women in hemophilia, including their carrier status, bleeding symptoms, treatment challenges, and psychosocial impact not only related to male patients, but also as patients affected with hemophilia themselves. We advocate health equity, equal access to healthcare for men and women with hemophilia and dedicated resources to improve the unique needs of the women dealing with hemophilia, ultimately leading to improved care and quality of life.
Keywords: bleeding symptoms; carrier; gender-specific research; hemophilia; psychosocial impact; quality of life; treatment challenges; women.
Copyright © 2024 Gualtierotti, Garagiola, Mortarino, Spena, Romero-Lux and Peyvandi.
Conflict of interest statement
RG advisory board of Bayer, Roche; speaker bureau/educational meetings Pfizer, SOBI, Takeda, Novo Nordisk; FP advisory board of CSL Behring, Biomarin, Roche, Sanofi, Sobi; speaker bureau/educational meetings Takeda/Spark. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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