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Caregiver Perspectives: Jackie and Colin, Primary Hyperoxaluria Type 1 (PH1)
Автор: Alnylam Pharmaceuticals
Загружено: 2025-04-17
Просмотров: 444
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This video was created for CEMEA audiences.
As a newborn, Ziggy was diagnosed with primary hyperoxaluria type 1 (PH1)—a rare, inherited disease that causes the overproduction of oxalate, which builds up as crystals throughout the body. Watch Ziggy’s parents, Jackie and Colin, discuss their family’s experience navigating life with PH1.
NP-INTX-00176
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