Korean J Nephrol.  2000 Jul;19(4):760-764.

A Case of Alport's Syndrome in an Adult

Affiliations
  • 1Department of Internal Medicine, Chonbuk National University Medical school, Chonju, Korea.
  • 2Institutes for medical Sciences, Chonbuk National University Medical school, Chonju, Korea.
  • 3Department of Pathology, Chonbuk National University Medical school, Chonju, Korea.

Abstract

Alport's syndrome is a progressive hereditary kidney disease. The disease is primarily X chromosome- linked but autosomal forms have also been reported. The authors experienced a case of Alport's syndrome in a 19-year-old man who showed persistent hematuria and proteinuria. The diagnosis was based on the presence of hematuria on the pedigree of patient's maternal site and characteristic electron microscopic findings of renal tissue, and persistent hematuria. There was, however, no abnormal finding on audiogram and eye exami-nation. We report this case with a review of literature.

Keyword

Alport's syndrome; Hematuria; Proteinuria

MeSH Terms

Adult*
Diagnosis
Hematuria
Humans
Kidney Diseases
Nephritis, Hereditary*
Pedigree
Proteinuria
Young Adult
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