Nielsen C E
Acta Ophthalmol (Copenh). 1978;56(4):518-30. doi: 10.1111/j.1755-3768.1978.tb01365.x.
Six patients, from five families, five males and one female, suffering from lenticonus anterior are presented. Furthermore, all suffered from chronic nephritis and nerve deafness and must be considered cases of Alport's syndrome. As all cases with lenticonus anterior which have been published within the last 13 years likewise were affected with nerve deafness and/or chronic nephritis, the assumption is submitted that lenticonus anterior exists exclusively as a part of Alport's syndrome. It is pointed out that four patients had a weakened bilateral macula reflex with changes in pigmentation. Attention is drawn to the fact that patients with lenticonus anterior often have a cornea astigmatism of 2-3 D. A complete table of all reported patients with anterior lenticonus is presented.
本文报告了来自五个家庭的六例患者,五男一女,均患有前圆锥形晶状体。此外,所有患者都患有慢性肾炎和神经性耳聋,应被视为阿尔波特综合征病例。由于过去13年内发表的所有前圆锥形晶状体病例同样都伴有神经性耳聋和/或慢性肾炎,因此提出一种假设,即前圆锥形晶状体仅作为阿尔波特综合征的一部分存在。指出有四名患者双侧黄斑反射减弱且伴有色素沉着变化。需注意的是,前圆锥形晶状体患者通常有2 - 3 D的角膜散光。文中给出了所有已报告的前圆锥形晶状体患者的完整表格。