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  • Alport Syndrome: Causes, Symptoms Treatment - Cleveland Clinic
    Alport syndrome is a condition that affects your kidneys Mutations in your collagen genes cause Alport syndrome Symptoms include blood and protein in your pee and hearing and vision loss It may also cause kidney failure Treatment often includes ACE inhibitors and ARBs
  • Alport Syndrome | National Kidney Foundation
    Alport syndrome is a disease that damages the tiny blood vessels in your kidneys It can lead to kidney disease and kidney failure It can also cause hearing loss and problems within the eyes
  • Alport syndrome: MedlinePlus Genetics
    Alport syndrome is a genetic condition characterized by kidney disease, hearing loss, and eye abnormalities Explore symptoms, inheritance, genetics of this condition
  • Alport Syndrome - Symptoms, Causes, Treatment | NORD
    Alport syndrome is a rare genetic disorder characterized by progressive kidney disease and abnormalities of the inner ear and the eye There are three genetic types X-linked Alport syndrome (XLAS) is the most common; in these families affected males typically have more severe disease than affected females
  • Alport Syndrome - GeneReviews® - NCBI Bookshelf
    Alport syndrome is characterized by kidney manifestations, sensorineural hearing loss (SNHL), and ocular manifestations
  • Alport Syndrome Patient Guide
    Alport syndrome affects the kidneys and may progress to kidney failure regardless of sex assigned at birth It also may cause hearing loss and or changes to the eyes Alport syndrome uniquely impacts individuals based on a number of factors, such as genetics
  • Explaining Alport syndrome—lessons from the adult nephrology clinic
    Alport syndrome is an inherited kidney disease that affects the glomeruli, is often progressive, and may be associated with sensorineural hearing loss and eye abnormalities This article focusses on this collection of conditions called ’Alport syndrome’
  • Alport Syndrome - Genitourinary Disorders - MSD Manual Professional Edition
    Alport syndrome is a genetically heterogeneous disorder characterized by nephritic syndrome (ie, hematuria, proteinuria, hypertension, eventual chronic kidney disease) often with sensorineural deafness and, less commonly, ophthalmologic symptoms Cause is a gene mutation affecting type IV collagen





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