Cameron J A
King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
Cornea. 1993 Jan;12(1):54-9. doi: 10.1097/00003226-199301000-00009.
Eleven patients with blue sclera, limbus-to-limbus corneal thinning, hypermobile joints, and consanguineous parents were examined between January 1983 and September 1991. The clinical diagnosis was consistent with the Ehlers-Danlos syndrome type VI phenotype in all patients. A "halo" sign at the limbus was present in all patients. Corneal rupture occurred in seven patients (nine eyes) either spontaneously or following minimal trauma. Acute hydrops occurred in three patients. Bilateral microcornea was present in one patient and two patients had a unilateral increased corneal diameter as a result of secondary glaucoma after trauma. Peripheral sclerocornea was present bilaterally in five patients. Curvature abnormalities included cornea plana, keratoconus, and keratoglobus.
1983年1月至1991年9月期间,对11例患有蓝色巩膜、角膜从边缘到边缘变薄、关节活动过度且父母为近亲的患者进行了检查。所有患者的临床诊断均与Ⅵ型埃勒斯-当洛综合征的表型一致。所有患者角膜缘均出现“晕轮”征。7例患者(9只眼)发生角膜破裂,破裂情况或是自发的,或是在受到轻微创伤后出现。3例患者发生急性角膜水肿。1例患者出现双侧小角膜,2例患者因外伤后继发性青光眼导致单侧角膜直径增大。5例患者双侧出现周边巩膜角膜。曲率异常包括扁平角膜、圆锥角膜和球形角膜。