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Get the free Patients with Fabry disease on dialysis in the United States ...

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Washington University in St. Louis, Nephrology Home Dialysis Curriculum 20192020Staff Dr. Daniel Cone Dr. George Jared Dr. Channel Hours Dr. Tinting Li Dr. Anubhav Guinea Dr. Frank O'Brien Dr. Marcos
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Gather all necessary patient information such as personal details, medical history, and family history.
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Conduct a physical examination to assess the patient's overall health condition.
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Perform specific diagnostic tests such as genetic testing or enzyme testing to confirm the diagnosis of Fabry disease.
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Consult with specialists such as a geneticist or nephrologist to ensure accurate diagnosis and appropriate treatment plan.
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Develop a comprehensive treatment plan that may include enzyme replacement therapy, pain management, and regular follow-up visits.
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Educate the patient and their family about Fabry disease, its symptoms, and the importance of adherence to treatment.
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Provide ongoing support and counseling to help the patient cope with the challenges of living with Fabry disease.

Who needs patients with fabry disease?

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Patients who have been diagnosed with Fabry disease or are suspected of having the condition.
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Fabry disease is a genetic disorder that results from the buildup of a certain type of fat, called globotriaosylceramide, due to a deficiency of the enzyme alpha-galactosidase A. This condition can lead to various symptoms, including pain, skin rashes, kidney problems, and heart issues.
Healthcare providers and specialists who treat patients diagnosed with Fabry disease are typically required to file relevant patient information to appropriate registries or health authorities.
To fill out information for patients with Fabry disease, healthcare providers should gather relevant patient data including medical history, symptoms, laboratory results, and treatment plans, ensuring accurate and comprehensive reporting.
The purpose of managing patients with Fabry disease includes monitoring disease progression, facilitating access to treatment, supporting clinical research, and improving patient outcomes through targeted therapies.
Information that must be reported includes patient demographics, clinical symptoms, biochemical test results, imaging studies, treatment history, and any complications related to Fabry disease.
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