The topic Hemorrhagic Familial Nephritis you are seeking is a synonym, or alternative name, or is closely related to the medical condition Alport Syndrome.

Quick Summary:

• Alport Syndrome is a genetic disorder that is characterized by damage to the blood vessels in the kidneys, resulting in nephritis (kidney inflammation) and progressive kidney failure
• As the disorder progresses, kidney disease, hearing loss, and vision-related abnormalities are likely to occur. Complications of Alport Syndrome are end-stage kidney failure, blindness, and vision loss
• Mutations in the genes coding for collagen production are responsible for the symptoms associated with Alport Syndrome. Collagen is important for forming blood vessels in the kidneys; these vessels (glomeruli) remove water and waste from blood and create urine. When mutations are present, collagen is not produced appropriately and the blood vessels cannot function properly
• The diagnosis of Alport Syndrome may include a urine test, serum levels of urea and creatinine, and a renal biopsy
• There is no cure of Alport syndrome; the treatment is aimed at managing the symptoms. The condition cannot also be effectively prevented
• Males are more commonly affected by Alport Syndrome than females; also, females have a milder condition than males. Women with Alport Syndrome have better prognosis than men

Please find comprehensive information on Alport Syndrome regarding definition, distribution, risk factors, causes, signs & symptoms, diagnosis, complications, treatment, prevention, prognosis, and additional useful information HERE.