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STUDY NAME: Rare Kidney Disease (RKD) Registry and Biobank Information Leaflet and Consent Form for VASCULITIS PATIENTS Site:Cork University HospitalPrincipal Investigator (PI):Dr Michael ClarksonContact
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Gather all necessary information about the patient's medical history, including their previous diagnoses, treatments, and medications.
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Rare kidney disease (RKD) refers to a group of uncommon disorders affecting the kidneys, which may lead to significant health issues, renal failure, and often require specialized treatment.
Healthcare providers, researchers, and organizations involved in rare kidney disease diagnosis, treatment, or research may be required to file reports related to RKD.
Filling out the rare kidney disease RKD form typically involves providing patient information, diagnosis details, treatment plans, and outcomes based on established guidelines provided by health authorities.
The purpose of reporting RKD is to enhance understanding of these diseases, improve patient care, track prevalence, and facilitate research efforts in the field.
Reported information on RKD may include patient demographics, clinical findings, treatment details, diagnostic tests, and follow-up results.
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