Mvogo C E, Ellong A, Bella-Hiag A L, Luma-Namme H
Service d'opthtalmologie de l'hôpital général de Douala, BP 4856, Douala, Cameroun.
Sante. 2001 Oct-Dec;11(4):237-9.
This retrospective study took place in the Ophthalmology Department of Douala General Hospital. The aim was to determine the importance of hereditary factors in a group of strabismic Cameroonians. In a series of 275 patients with strabismus, we found 79 familial cases (28.72%). Among them, 22.78% had more than one relative with squint and 75% had the same type of strabismus as their relative. There was no significant difference in the percentage of familial cases with regard to the type of strabismus, the sex, the mode of fixation and the impairment of ductions. As far as ametropias are concerned, only myopia showed a hereditary tendency in our series. The authors agree with the literature in that there is a significant hereditary component in the cause of strabismus, but its genetic sites are yet to be identified. There is strong hope in this direction with the decoding of the human genom and the advances in molecular biology. However, the study of familial cases is important since it allows high risk groups to be defined and screened. It thus makes it possible to successfully fight amblyopia through early detection and treatment.
这项回顾性研究在杜阿拉总医院眼科进行。目的是确定遗传因素在一组喀麦隆斜视患者中的重要性。在275例斜视患者系列中,我们发现79例家族性病例(28.72%)。其中,22.78%有不止一位亲属患有斜视,75%与亲属患有相同类型的斜视。家族性病例的百分比在斜视类型、性别、注视方式和眼球运动障碍方面无显著差异。就屈光不正而言,在我们的系列中只有近视显示出遗传倾向。作者认同文献观点,即斜视病因中存在显著的遗传成分,但尚未确定其基因位点。随着人类基因组的解码和分子生物学的进展,在这个方向上有很大希望。然而,对家族性病例的研究很重要,因为它可以确定和筛查高危人群。因此,通过早期发现和治疗有可能成功对抗弱视。