Atypical Hemolytic Uremic Syndrome

Overview

An hereditary hemolytic uremic syndrome associated with variations in the gene that encodes COMPLEMENT FACTOR H, or the related proteins CFHR1 and CFHR3. Disease often progresses to CHRONIC KIDNEY FAILURE without the prodromal symptoms of ENTEROCOLITIS and DIARRHEA that characterize typical hemolytic uremic syndrome.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Atypical Hemolytic Uremic Syndrome

Topic type

Condition

Category

Urology / Fertility

MeSH classification

C12.050.351.968.419.936.463.500|C12.200.777.419.936.463.500|C12.950.419.936.463.500|C15.378.050.141.610.500|C15.378.140.855.925.500.500|C15.378.243.937.925.500.500

Preparing for an appointment about Atypical Hemolytic Uremic Syndrome

If you are speaking with a healthcare professional about Atypical Hemolytic Uremic Syndrome, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

Finding care related to Atypical Hemolytic Uremic Syndrome

EuroCareFinder helps patients explore clinics and healthcare providers across Europe. Some topics link directly to services offered by clinics, while others may be connected through related specialties, treatments or procedures.

Related topics

Explore healthcare providers

Use EuroCareFinder to browse clinics by country, specialty and available services.