Expression of adult polycystic renal disease in a 17-year-old male
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is found mostly in the middle-aged group. We report a rare occurrence of ADPKD in a 17-year-old male student with clinical presentation of bilateral loin pains and total haematuria. Clinical diagnosis of Acute-on-Chronic Glomerulonephritis was mad...
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Published in: | West African journal of medicine Vol. 25; no. 2; pp. 164 - 165 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Nigeria
01-04-2006
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Subjects: | |
Online Access: | Get full text |
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Summary: | Autosomal Dominant Polycystic Kidney Disease (ADPKD) is found mostly in the middle-aged group. We report a rare occurrence of ADPKD in a 17-year-old male student with clinical presentation of bilateral loin pains and total haematuria. Clinical diagnosis of Acute-on-Chronic Glomerulonephritis was made. However Ultrasound and Intravenous Urography confirmed the diagnosis of Adult Polycystic Disease. The possible embryogenesis and associated anomalies of ADPKD and the radiological findings were reviewed. |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 0189-160X |