Marchesani’s综合征,及双眼性球形晶体及晶体异位,伴晶体性近视及青光眼。身材矮小,肢指(趾)短粗为特征的遗传性家族性疾病。本病1939年首先由Marchesani氐描述,故名。发病原因,可能是先天性中胚叶组织增生或增生的中胚叶营养障碍所致。本病少见,国内外报道者不满百例,国内仅数例。我院1978年曾遇一家姐妹四人皆患此病,且较典型,现报告如下。 Marchesani’s syndrome, and binocular spherical and crystalline ectopic, with accompanying myopia and glaucoma. Short stature, limbs (toes) short stature is characterized by hereditary familial diseases. The disease was first described by Marchesani in 1939, hence the name. The etiology may be due to congenital mesodermal tissue proliferation or proliferation of mesodermal nutrition disorders. The rare disease, domestic and foreign reporters dissatisfied with a hundred cases, only a few cases. Our hospital in 1978 encountered a sister and four are suffering from the disease, and more typical, are as follows.