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Alport syndrome

ORPHA:63· ICD-10 Q87.8

Definition

A rare renal disease characterized by glomerular nephropathy with hematuria progressing to end-stage renal disease (ESRD), frequently associated with sensorineural deafness, and occasionally with ocular anomalies.

Prevalence
Unknown
Inheritance
Autosomal dominant, Autosomal recessive, X-linked dominant
Age of onset
Adolescent, Adult, Childhood, Elderly