Fabry's disease is an X-linked disorder that manifests differently in men and women, leading to differences in healthcare pathways. In women, the disease is sometimes diagnosed through family screening despite the presence of symptoms (symptoms appear later than in men, and the phenotypic expression of the disease is sometimes more subtle). Conversely, in men, the presence of symptoms combined with abnormalities in medical examinations facilitates diagnosis. There is limited data on the differences in healthcare pathways between men and women, which could nevertheless impact diagnosis by identifying a profile of at-risk patients, and consequently, their management. The goal of this present study is to describe the differences in care pathways between men and women with Fabry's disease, distinguishing entry via symptoms or family screening through a non-interventional study based on a questionnaire sent to patients and on the collection of medical data at the time of diagnosis.
Study Type
OBSERVATIONAL
Enrollment
200
Medical data of Fabry's disease
Service de Cardiologie - 1 Avenue du Professeur Jean Poulhès
Toulouse, Occitanie, France
Diagnostic time in care pathways between men and women with Fabry's disease
The average diagnostic time, compared between men and women, and the diagnostic methods (entry point into the disease), compared according to sex.
Time frame: 8 months
Comparison of diagnostic methods between men and women
Data collection at the point of entry into the disease: via symptoms or family screening
Time frame: 8 months
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