Searching for Alport Syndrome Support information? Find all needed info by using official links provided below.
https://www.alportsyndrome.org/
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https://ghr.nlm.nih.gov/condition/alport-syndrome
Oct 01, 2019 · Alport syndrome is a genetic condition characterized by kidney disease, hearing loss, and eye abnormalities.. People with Alport syndrome experience progressive loss of kidney function. Almost all affected individuals have blood in their urine (hematuria), which indicates abnormal functioning of …
welcome to alport uk. alport uk is a patient-led organisation dedicated to empowering people living with Alport Syndrome to enjoy the best possible quality of life. Drawing on our continuous learning from and collaboration with individuals, families and the scientific community, this website aims to facilitate a support and information network for all those affected by Alport Syndrome.
https://alport.org.au/support/
Becoming part of the Alport Foundation’s community is so important to reduce the feelings of distress, isolation and uncertainty that can come from living with Alport Syndrome. Become a member of the Alport Foundation of Austraila’s network. Together we can support each other and make a difference.
Alport Syndrome is a genetic disease of the kidneys, which can also affect the inner ear and eye. It is inherited, and estimated to affect at least 1 in 5,000 people. Limited access to expensive genetic testing means the actual number of people with this hereditary disease is unknown.
https://www.cancertherapyadvisor.com/home/decision-support-in-medicine/labmed/alport-syndrome-2/
Alport syndrome is one of the many familial glomerulonephritis (GN). Often, this is seen as a GN (hematuria and proteinuria) in males, but only microscopic hematuria in females (carriers of the ...Author: Timothy Bunchman
https://rarediseases.info.nih.gov/diseases/5785/alport-syndrome
52 rows · Mar 18, 2017 · Alport syndrome is a genetic condition characterized by kidney disease, …
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