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- IgAN
IgAN occurs when an abnormal protein damages the filtering unit (glomerulus) inside the kidneys It is estimated that 20-40% of the people who have IgAN will develop end-stage kidney disease, which means they will need dialysis or kidney transplantation to survive
- IgANCare Program | IgA Nephropathy Foundation
There is an urgent need to raise awareness about IgAN, including how it differs from other chronic kidney conditions, and to help assure more timely diagnoses Nearly half of patients (48%) faced delays before being correctly diagnosed with IgAN
- Tools Resources | IgA Nephropathy Foundation
As a part of our patient-centric mission focused on finding a cure for IgA Nephropathy and supporting IgAN Warriors, the resources below are designed to help equip and empower you through every part of your treatment journey
- Diagnosed with IgA Nephropathy? What You Need to Know
Visit igan org for more information on specific medications that are used Here you will find a worksheet to keep track of your medications and treatments you’ve tried before
- What is IgA Nephropathy? [Immunoglobulin A (IgA)] Learn Here
IgAN occurs when an abnormal protein damages the filtering unit (glomerulus) inside the kidneys It is estimated that 20-40% of the people who have IgAN will develop end-stage kidney disease, which means they will need dialysis or kidney transplantation to survive
- IgAN FAQs
There is no current cure for IgAN and that is why the IgA Nephropathy Foundation was founded Since the disease varies from one person to another, there is no definite progression or course that the disease will take
- Clinical Trials - IgAN
The APRICOT study is an open-label, single-arm, multicenter Phase III clinical trial designed to evaluate the efficacy, pharmacokinetics, safety, and tolerability of iptacopan in pediatric patients aged 2 to under 18 years with primary immunoglobulin A nephropathy (IgAN)
- Go Global Australia | IgA Nephropathy Foundation
IgAN isn’t rare — it’s one of Australia’s most common and serious kidney diseases More awareness, research, and support are urgently needed for patients and families
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