Gilbert J, Clark R D, Koyle M A
Department of Surgery (Urology), Harbor/UCLA Medical Center, Torrance.
J Urol. 1990 Feb;143(2):338-9. doi: 10.1016/s0022-5347(17)39953-6.
Two male neonates (46XY karyotype) were born with a triad of penile agenesis associated with imperforate anus and complete absence of the median raphe. Both patients died of renal dysplasia and secondary pulmonary hypoplasia shortly after birth. This triad appears to be secondary to a lack of caudal mesoderm migration during month 1 of gestation, leading to severe developmental defects in the caudal axis. In all reported cases to date this triad of findings has been incompatible with extrauterine life.
两名男性新生儿(核型为46XY)出生时伴有阴茎发育不全、肛门闭锁和正中缝完全缺失的三联征。两名患者均在出生后不久死于肾发育不全和继发性肺发育不全。这种三联征似乎是由于妊娠第1个月时尾侧中胚层迁移缺乏所致,导致尾轴严重发育缺陷。在迄今为止所有报道的病例中,这一三联征的表现均与宫外生活不相容。