Kumar R, Pereira B J, Sakhuja V, Chugh K S
Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Clin Genet. 1989 Mar;35(3):202-4. doi: 10.1111/j.1399-0004.1989.tb02928.x.
A patient with familial angiolipomatosis in whom an autosomal dominant mode of inheritance could be established is described. This patient also had coincidental autosomal dominant polycystic kidney disease.
本文描述了一位可确定为常染色体显性遗传模式的家族性血管脂肪瘤患者。该患者还同时患有常染色体显性多囊肾病。