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