Van Acker K J, Vincke H, Quatacker J, Senesael L, Van den Brande J
Arch Dis Child. 1971 Jun;46(247):321-6. doi: 10.1136/adc.46.247.321.
Four patients with oligonephronia are described. The clinical picture was that of a progressive renal insufficiency, but the time of onset and severity varied from one case to another. One patient had oligonephronia of one kidney and aplasia of the other kidney. In another patient a familial syndrome of multiple congenital anomalies was observed. In a sib of the latter patient, a simple unilateral renal hypoplasia was discovered.
本文描述了4例肾单位过少患者。临床表现为进行性肾功能不全,但发病时间和严重程度因病例而异。1例患者一侧肾肾单位过少,另一侧肾发育不全。另1例患者观察到一种伴有多种先天性异常的家族综合征。在该患者的1名同胞中,发现了单纯性单侧肾发育不全。