Alport's syndrome
Last reviewed 09/2021
Alport's syndrome is a hereditary disease of basement membranes which is characterised by sensorineural deafness and renal failure.
Inheritance can be X-linked dominant, autosomal dominant and, rarely, autosomal recessive. More information about the genetics of this condition is available in the linked menu item.
Prevalence is about 1:5000.
Pathological renal changes in Alport's syndrome include thickening of the glomerular basement membrane and splitting of the lamina densa.