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Marchesani综合征是一种常染色体的遗传性疾病,自well和Marchesahi(1939)报导以后,国内到1982年止已报导了12例。但Marchesani综合征伴斜症者国内外均未见有报导,现把我院收治兄弟俩患Marchesani综合征伴先天性腹股沟斜病报导如下: 例1:患者类××,男性,26岁(市)农住院号35356 主诉:又眼视物模糊不清十余年加重三年。现病史;十余年前自懂事起即觉双眼视物不清,近三年加重且时有双眼痛,视力下降以致不能参加日常劳动,仅能见人影而分不清五官。否认有双眼和病史。智力发育差,从小右侧阴囊触及可复性囊块,未经治疗。父母系姑表兄妹近亲联姻。
Marchesani syndrome is an autosomal genetic disease, reported by well and Marchesahi (1939), until the end of 1982, 12 cases have been reported in China. Marchesani syndrome, but there are no reports of both at home and abroad, Marchesani syndrome is now reported in our hospital now admitted to the two brothers with Marchesani syndrome with congenital inguinal canal disease reported as follows: Example 1: patients × ×, male, 26 years old ) Rural Hospital No. 35356 Chief Prosecutor: Also blurred vision more than ten years aggravate three years. History of the present illness; more than ten years ago, self-consciously perceived from both eyes blurred vision, the past three years increased and sometimes have both eyes pain, visual acuity so that they can not participate in daily work, can only see the shadow and can not distinguish facial features. Denied having both eyes and medical history. Poor mental development, from the right side of the scrotum touches reusable sac, untreated. Parents cousins cousin marriage.