Rabinowitz R, Schillinger J F
J Urol. 1977 Sep;118(3):454-6. doi: 10.1016/s0022-5347(17)58056-8.
The prune belly syndrome of marked abdominal muscle deficiency and associated genitourinary anomalies has been found almost exclusively in male subjects. Of the few reported cases of female patients with this entity most are questionable or incomplete forms. The light microscopic histology and electron microscopic ureteral abnormalities in male subjects have been reported previously. A female newborn with marked abdominal muscle deficiency and severe bilateral ureteropyelocaliectasis is described. Chromosomal studies showed 46 XX karyotype. Histologic examination of the ureter by light microscopy was compatible with the diagnosis.
几乎仅在男性患者中发现了伴有明显腹肌缺如及相关泌尿生殖系统异常的梅干腹综合征。在少数报道的患有该病症的女性患者中,大多数病例存在疑问或为不完整形式。此前已有关于男性患者的光镜组织学及输尿管电镜异常的报道。本文描述了一名患有明显腹肌缺如及严重双侧输尿管肾盂扩张的女性新生儿。染色体研究显示其核型为46 XX。输尿管的光镜组织学检查结果与诊断相符。