Fujiwara H, Takigawa Y, Ueno S, Okuda K
Department of Ophthalmology, Kawasaki Hospital, Kawasaki Medical School, Japan.
Br J Ophthalmol. 1990 Oct;74(10):631-4. doi: 10.1136/bjo.74.10.631.
The Weill-Marchesani syndrome is a rare systemic connective tissue disease characterised by small stature, brachydactyly, ectopia lentis, and spherophakia. Three siblings with typical manifestations of this syndrome were reported. The ophthalmological findings in all these cases were spherophakia, severe myopia, a shallow anterior chamber, and narrow angle glaucoma. Two cases underwent laser iridotomy and drug treatment. In the third case the lens was removed from the eye because of injury, and this lens was examined by light and electron microscopy.
Weill-Marchesani综合征是一种罕见的全身性结缔组织疾病，其特征为身材矮小、短指畸形、晶状体异位和球形晶状体。本文报道了3例具有该综合征典型表现的同胞患者。所有这些病例的眼科检查结果均为球形晶状体、高度近视、前房浅和窄角型青光眼。2例患者接受了激光虹膜切开术和药物治疗。第3例患者因眼部受伤而摘除了晶状体，并对该晶状体进行了光镜和电镜检查。
