
We review Alport's syndrome based on the description of seven members of a family whose disease was confirmed by percutaneous biopsy of renal specimens. The importance of genetic counseling and of the prophylaxis of hearing losses through cochlear protection is emphasized.
Adult, Male, Adolescent, Child, Preschool, Humans, Infant, Female, Nephritis, Hereditary, Child, Hearing Disorders
Adult, Male, Adolescent, Child, Preschool, Humans, Infant, Female, Nephritis, Hereditary, Child, Hearing Disorders
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