Journal of the Korean Pediatric Society 1995;38(8):1151-1154.
Published online August 15, 1995.
A Case Report of Acrorenal Syndrome
Soo Hee Chang, Jo Seph Choi, Soo Chul Cho, Dae Yeol Lee
Department of Pediatrics, Chonbuk National University Medical School, Chonju, Korea
Acrorenal Syndrome 1례
장수희, 최요섭, 조수철, 이대열
전북대학교 의과대학 소아과학교실
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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