Alport Syndrome Quiz

Check your symptoms and
find possible causes with AI for free

Reviewed By:

Yoshinori Abe, MD

Yoshinori Abe, MD (Internal medicine)

Dr. Abe graduated from The University of Tokyo School of Medicine in 2015. He completed his residency at the Tokyo Metropolitan Health and Longevity Medical Center. He co-founded Ubie, Inc. in May 2017, where he currently serves as CEO & product owner at Ubie. Since December 2019, he has been a member of the Special Committee for Activation of Research in Emergency AI of the Japanese Association for Acute Medicine. | | Dr. Abe has been elected in the 2020 Forbes 30 Under 30 Asia Healthcare & Science category.

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With an easy 3-min questionnaire, Ubie's AI-powered system will generate a free report on possible causes.

  • Trained and reviewed by 50+ doctors, our AI Symptom Checker utilizes data from 1,500+ medical centers

  • Questions are customized to your situation and symptoms

  • Alport syndrome as well as similar diseases can be checked at the same time.

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✔︎  When to see a doctor

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People with similar symptoms also use Ubie's symptom checker to find possible causes

  • Blood from the urethra

  • Bloody urine

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Learn more about Alport syndrome

Content updated on Nov 2, 2022

What is alport syndrome?

A rare genetic disorder characterized by progressive kidney disease and abnormalities of the inner ear and the eye.

Symptoms of alport syndrome

  • Bloody or red urine

Questions your doctor may ask to check for alport syndrome

Your doctor may ask these questions to diagnose alport syndrome

  • Have you ever had red or brown urine (hematuria)?

Treatment for alport syndrome

The treatment is directed toward the specific symptoms that are apparent in each individual. Angiotensin-converting enzyme (ACE inhibitor) therapy or angiotensin receptor blockers (ARB) therapy may reduce protein in urine and the progression of kidney disease.

View the symptoms of Alport syndrome

  • Blood in urine

References

  • Kashtan CE. Alport Syndrome: Achieving Early Diagnosis and Treatment. Am J Kidney Dis. 2021 Feb;77(2):272-279. doi: 10.1053/j.ajkd.2020.03.026. Epub 2020 Jul 22. PMID: 32712016.

    https://www.ajkd.org/article/S0272-6386(20)30734-4/fulltext

  • Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K. A review of clinical characteristics and genetic backgrounds in Alport syndrome. Clin Exp Nephrol. 2019 Feb;23(2):158-168. doi: 10.1007/s10157-018-1629-4. Epub 2018 Aug 20. PMID: 30128941; PMCID: PMC6510800.

    https://link.springer.com/article/10.1007/s10157-018-1629-4

  • Savige J, Ariani F, Mari F, Bruttini M, Renieri A, Gross O, Deltas C, Flinter F, Ding J, Gale DP, Nagel M, Yau M, Shagam L, Torra R, Ars E, Hoefele J, Garosi G, Storey H. Expert consensus guidelines for the genetic diagnosis of Alport syndrome. Pediatr Nephrol. 2019 Jul;34(7):1175-1189. doi: 10.1007/s00467-018-3985-4. Epub 2018 Jul 9. PMID: 29987460.

    https://link.springer.com/article/10.1007/s00467-018-3985-4

  • Torra R, Furlano M. New therapeutic options for Alport syndrome. Nephrol Dial Transplant. 2019 Aug 1;34(8):1272-1279. doi: 10.1093/ndt/gfz131. PMID: 31190059.

    https://academic.oup.com/ndt/article/34/8/1272/5514265

User testimonials

Reviewed By:

Yoshinori Abe, MD

Yoshinori Abe, MD (Internal medicine)

Dr. Abe graduated from The University of Tokyo School of Medicine in 2015. He completed his residency at the Tokyo Metropolitan Health and Longevity Medical Center. He co-founded Ubie, Inc. in May 2017, where he currently serves as CEO & product owner at Ubie. Since December 2019, he has been a member of the Special Committee for Activation of Research in Emergency AI of the Japanese Association for Acute Medicine. | | Dr. Abe has been elected in the 2020 Forbes 30 Under 30 Asia Healthcare & Science category.

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