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  • Overview
    • Overview of Fabry disease
    • Epidemiology
    • Genetic Cause
    • X-linked Inheritance
  • Symptoms
    • General symptoms
    • Cardiac
    • Renal
    • Neurological
  • Diagnosis
    • Diagnostic Kits
    • Screening Populations
    • Fabry disease symptoms checklist
    • Establishing a diagnosis
    • Confirming a diagnosis
    • Importance of early diagnosis
    • Misdiagnosis
  • Management
    • Pedigree
    • Genetic counselling
    • Specific treatment
    • Symptomatic treatment
  • Information for patients
    • Useful brochures to understand Fabry disease
    • Useful links
  • FAQs
  • Diagnostic kits Form
Home » Patient Stories
 Gina’s Story: The long walk to a diagnosis
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By Rare2Aware
In Advocacy & Awareness, Angiokeratomas, Changes in the eye, Community, Fabry Disease, Hearing problems, Impaired ability to sweat, Patient Stories, Pedigree Analysis, Stomach problems
Posted May 3, 2016

Gina’s Story: The long walk to a diagnosis

Meet Gina, a 56-year old mother to E (Fabry patient), based in Ontario, Canada. After five years of jumping through hurdles she finally received a diagnosis of Fabry disease for her then [...]

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