Alport Syndrome Quiz
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Reviewed By:
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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Red-brown urine came out
Blood is mixed in pee
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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
Diseases related to Alport syndrome
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
Reviewed By:
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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Seiji Kanazawa, MD, PHD
Obstetrics and gynecology (OBGYN)
National Center for Child Health and Development, Japan