| A Case Report of Acrorenal Syndrome |
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Soo Hee Chang, Jo Seph Choi, Soo Chul Cho, Dae Yeol Lee |
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Department of Pediatrics, Chonbuk National University Medical School, Chonju, Korea |
| Acrorenal Syndrome 1례 |
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장수희, 최요섭, 조수철, 이대열 |
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전북대학교 의과대학 소아과학교실 |
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| Abstract |
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Acrorenal syndrome is congenital anomaly of the limbs and urinary tract of unknown etiology. Acral malformations consist of varying combinations of oligodactyly, ectrodactyly, syndactyly, brachydactyly, polydactyly, and carpal, tarsal, or metatarsal fusions of the hands and feet. Urinary tract abnormalities include unilateral renal agenesis and duplication of the collecting system. The condition is a polytopic developmental field defect(acrorenal field) and usually is sporadic.
This report descirbes a case of Acrorenal syndrome of ectrodactyly, brachydactyly, and syndactyly of left hand assocaited ipsilateral renal hypoplasia. |
| Key Words:
Acrorenal syndrome, Congenital anomaly, Limbs, Urinary tract |
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