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患儿男,新生儿期因脐部出血、膀胱出血、贫血在我院住院两次,诊断为家族性多凝血因子缺乏综合征(FMFD)、脐部出血、膀胱出血、失血性贫血,经治疗,患儿康复出院。由于FMFD临床少见,目前国内罕见报道,现报告如下。1临床资料第1次入院,生后8 d,因“脐部出血不止、肉眼血尿0.5 d”入院。患儿系G_2P_2,孕足月行剖宫产娩出,无窒息抢救史,Apgar评分、羊水、脐带均正常,出生体重3.3 kg。入我院前0.5 d患儿脐部出血不止且未在外院治疗,病
Children male, neonatal bleeding due to umbilical cord, bladder hemorrhage, anemia hospitalized twice in our hospital, diagnosed as familial poly coagulation factor deficiency syndrome (FMFD), umbilical hemorrhage, bladder hemorrhage, hemorrhagic anemia, after treatment , Children were discharged from hospital. As FMFD clinical rare, rarely reported at home, the report is as follows. 1 clinical data of the first admission, 8 days after birth, because “Umbilical bleeding more than gross hematuria 0.5 d ” admission. Children with G_2P_2, pregnancy full term cesarean section delivery, no asphyxia rescue history, Apgar score, amniotic fluid, umbilical cord were normal, birth weight 3.3 kg. Into our hospital before 0.5 d bleeding in children with umbilical and not outside the hospital treatment, disease