Bagheri Mansooreh, Farvardin Majid, Saadat Mostafa
Poostchi Eye Research Center, Department of Ophthalmology, Shiraz University of Medical Sciences, Zand Avenue, Shiraz, Iran.
J Community Genet. 2015 Apr;6(2):177-80. doi: 10.1007/s12687-015-0213-9. Epub 2015 Feb 3.
Inheritance has an important role in the etiology of comitant strabismus. Consanguineous marriage is a leading factor in birth defects in which inheritance has a role. The aim of this study is to reveal if consanguineous marriage increases the risk of developing comitant strabismus. We included 461 patients who underwent primary surgery for comitant strabismus in Shiraz University Khalili Hospital (Fars province, southern Iran) between years 2003 and 2013 in our study. All the patients were living in Shiraz, Iran. Patients were categorized into the following 4 groups: (1) intermittent or constant exotropia, (2) infantile esotropia, (3) non-accommodative acquired esotropia, and (4) accommodative acquired esotropia. A total of 421 healthy children who were born in Shiraz, at the same period of time, were also studied as a control group. Presence and type of the consanguineous marriages were evaluated in the parents of the patients and control group by a questionnaire. Mean of inbreeding coefficient (α) was calculated in each group of patients and was compared with those of control group. The proportion of parental first cousin marriage was 37.7 and 23.5 % among patient and control groups. The mean of inbreeding coefficients (α) were 0.0236, 0.0283, 0.0288, and 0.0236 in four groups of the patients, respectively. The mean of inbreeding coefficient was 0.0263 in total patients, which was significantly higher than 0.0164 of control group (T = 5.27, df = 880, P < 0.001). Patients with non-accommodative acquired esotropia had the highest mean of inbreeding coefficient (α) (0.0288). It seems that recessive form of inheritance plays an important role in the etiology of comitant strabismus. Modified screening programs may be needed for earlier detection of strabismus in the offspring of consanguineous couples.
遗传在共同性斜视的病因中起着重要作用。近亲结婚是出生缺陷的一个主要因素,而遗传在其中发挥了作用。本研究的目的是揭示近亲结婚是否会增加患共同性斜视的风险。我们纳入了2003年至2013年间在设拉子大学哈利利医院(伊朗南部法尔斯省)接受共同性斜视初次手术的461例患者。所有患者均居住在伊朗设拉子。患者被分为以下4组:(1)间歇性或恒定性外斜视;(2)婴儿型内斜视;(3)非调节性后天性内斜视;(4)调节性后天性内斜视。同时,还对同一时期在设拉子出生的421名健康儿童作为对照组进行了研究。通过问卷调查评估患者组和对照组父母中近亲结婚的情况及类型。计算每组患者的平均近亲系数(α),并与对照组进行比较。患者组和对照组中父母为第一代堂兄妹结婚的比例分别为37.7%和23.5%。4组患者的平均近亲系数(α)分别为0.0236、0.0283、0.0288和0.0236。所有患者的平均近亲系数为0.0263,显著高于对照组的0.0164(T = 5.27,自由度 = 880,P < 0.001)。非调节性后天性内斜视患者的平均近亲系数(α)最高(0.0288)。看来隐性遗传形式在共同性斜视的病因中起重要作用。可能需要改进筛查方案,以便更早地发现近亲夫妇后代中的斜视。