Alport. Alport syndrome is a genetic disorder that is characterized by glomerulonephritis, often in combination with sensorineural hearing loss and sometimes eye abnor… Alport syndrome is an X-linked dominant disorder that is characterized by a mutation in type IV collagen. The term Alport syndrome refers to a group of inherited, heterogeneous disorders involving the basement membranes of the kidney and frequently affecting the cochlea and eye as well.
Alport Syndrome is a genetic disease of the kidneys, which can also affect the inner ear and eye. Alport syndrome is caused by disease-causing variants in the DNA sequences of specific genes. Ponieważ Alport to producent wykonujący każde okno od podstaw, zgodnie z potrzebami klienta.
Alport syndrome is an X-linked dominant disease characterized by progressive sensorineural hearing loss, renal disease and, at times, ocular lesions.
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Stages of Kidney Disease in Alport Syndrome. Learn and reinforce your understanding of Alport syndrome through video. Alport syndrome is a rare genetic condition that results in inflammation and eventual failure of the kidneys.