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先天性大疱性表皮松懈症是一种少见的常染色体遗传性疾病。本院自1979年以来共收治12例,除2例自动出院外,余全部治愈出院。现报告如下。临床资料一、一般资料: 男9例,女3例。日龄为生后3小时～15天。皮损发现时间生时即有7例,生后1～11天5例。1例因头盆不称行剖腹产,余足月顺产。本组均无窒息史。体重2500～3500g,父母无近亲史。1例母孕3个月时患疟疾,经抗疟治疗。另一例孕期两下肢轻度水肿,原有高血压史,曾服降压药及钙片。1例其兄生后即患本病,数年来时轻时重,
Congenital bullous epidermis syndrome is a rare autosomal genetic disease. The hospital since 1979, a total of 12 cases were treated, except 2 cases were discharged automatically, I was all cured. The report is as follows. Clinical data First, the general information: 9 males and 3 females. Age of 3 hours after birth to 15 days. 7 cases of lesions found when the time of birth, 1 to 11 days after birth in 5 cases. 1 case due to cephalopelvic dispatched Caesarean section, after full delivery. This group had no history of asphyxia. Weight 2500 ~ 3500g, no history of close relatives. One case of maternal 3 months pregnant suffering from malaria, the anti-malaria treatment. Another case of mild edema of both lower extremities during pregnancy, the original history of hypertension, antihypertensive drugs and calcium tablets. 1 case of his brother suffering from the disease after the disease, over the years when light weight,