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증례 : 17 세에 말기신부전으로 진행된 상염색체 우성 다낭종신 ( ADPKD) 1 예 (A Case of ESRD Caused by ADPKD ( Autosomal Dominant Polycystic Kidney Disease ) in a 17 - year - old Patient) |
김진수(Jin Soo Kim),한병근(Byoung Guen Han),최승욱(Seung Ok Choi) |
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Abstract |
Autosomal dominant polycystic kidney disease (ADPKD) is probably the common human disorder inherited by an autosomal dominant mechanism with worldwide prevalence of 1 out of 500-1,000 individ- uals. Progressive decline in renal function is usual. Approximately 50 percent of ADPKD develops into ESRD by age of 60. However, developed ESRD is rare before age of 30. We experienced a case of ESRD caused by ADPKD. The patient is a 17-year- old male mainly complaining of known fatigue and general weakness. Clinical manifestations, laboratory data, ultrasonogram, abdominal CT scanning and pathologic findings of the kidney diagnosed it. A review of literatures was also briefly presented. |
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