Fabry Disease Patient Journey

Поделиться
HTML-код
  • Опубликовано: 7 июн 2024
  • Maya Kineen, a Fabry disease patient and advocate, provides a patient's perspective of her journey with this rare disorder.
    Fabry disease an X-linked genetic disorder that leads to the buildup of globotriaosylceramide in the body’s cells.
    Common features of Fabry disease include episodes of pain (acroparesthesias), angiokeratomas, hypohidrosis; corneal opacity, gastrointestinal problems, tinnitus, and hearing loss. Fabry disease also involves potentially life-threatening complications such as progressive kidney damage, heart attack, and stroke.

Комментарии •