Hjalmarson O, Sabel K G
Acta Paediatr Scand. 1978 Jan;67(1):121-3. doi: 10.1111/j.1651-2227.1978.tb16288.x.
A newborn infant with bilateral aplasia of kidneys and ureters and a rudimentary bladder is reported. Other manifestations of Potter's syndrome (oligohydramnios, lung hypoplasia and an abnormal face) were missing as were other congenital malformations. Deviations from the full picture of Potter's syndrome seem to be rare. This case, however, shows that bilateral renal aplasia cannot be excluded as a cause of anuria in a newborn infant, even if all other manifestations of Potter's syndrome are missing.
本文报道了一名患有双侧肾和输尿管缺如以及残余膀胱的新生儿。波特综合征的其他表现(羊水过少、肺发育不全和面部异常)均未出现,也未发现其他先天性畸形。波特综合征全貌的偏差似乎很少见。然而,该病例表明,即使波特综合征的所有其他表现均未出现,双侧肾缺如也不能排除是新生儿无尿的原因。