范可尼氏(Fanconi＇s)综合征是一种伴有先天畸形的骨髓增生低下性贫血综合征。我们收治8例,现报告如下。临床资料一、一般情况:8例中,男3例,女5例;年龄在2～10岁间。8例患者双亲中,有智力低下者8人,患有精神病者2人,有先天畸形者1人。二、临床表现:8例均发育落后,均呈贫血貌。智力低下者4例,眼间距增宽者4例,小眼者2例,耳廓畸形者3例,腭弓增高者5例,双手六指者1例,双足马蹄内翻者1例,心室间隔缺损者 Fanconi’s syndrome is a myelodysplastic anemia syndrome with congenital malformations. We admitted 8 cases, are as follows. Clinical data First, the general situation: 8 cases, 3 males and 5 females; aged 2 to 10 years old. Among the 8 parents, there were 8 persons with mental retardation, 2 with mental illness and 1 with congenital malformation. Second, the clinical manifestations: 8 cases were lagging behind, were anemic appearance. 4 cases of mental retardation, 4 cases of widened interocular distance, 2 cases of small eyes, 3 cases of auricular deformity, 5 cases of elevated palatal arch, 1 case of both hands and 6 fingers, 1 case of double-foot clubfoot, 1 case of ventricular Separation of defects