copy and paste this google map to your website or blog!
Press copy button and paste into your blog or website.
(Please switch to 'HTML' mode when posting into your blog. Examples: WordPress Example, Blogger Example)
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 - Wikipedia Alport syndrome is a genetic disorder [1] affecting around 1 in 5,000–10,000 children, [2] characterized by glomerulonephritis, end-stage kidney disease, and hearing loss [3]
Alport Syndrome | National Kidney Foundation Alport syndrome is a genetic disease causing kidney damage, hearing loss, and eye problems Learn about its symptoms, diagnosis, and treatments for kidney health
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 - Penn Medicine Alport syndrome is an inherited form of kidney inflammation (nephritis) It is caused by a defect (mutation) in a gene for a protein in the connective tissue, called collagen
Alport syndrome - American Kidney Fund (AKF) Alport syndrome is a genetic disease that primarily affects the kidneys but can also affect the eyes and ears, which can present as having hearing loss in one or both ears
Clinical manifestations, diagnosis, and treatment of Alport . . . - UpToDate Alport syndrome is a primary basement membrane disorder arising from pathogenic variants in genes encoding several members of the collagen IV protein family The clinical manifestations, diagnosis, and treatment of Alport syndrome will be reviewed here
Alport Syndrome Patient Guide Alport syndrome is considered a type of chronic kidney disease What causes Alport syndrome? Alport syndrome is caused by genetic mutations in a person’s DNA Individuals with Alport syndrome typically have defects in their COL4A3, COL4A4, or COL4A5 genes (or a combination of these)