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视神经发育不良的发病率及相关内分泌和神经学异常。

Incidence and associated endocrine and neurologic abnormalities of optic nerve hypoplasia.

机构信息

Department of Ophthalmology, Mayo Clinic and Mayo Foundation, Rochester, MN 55905, USA.

出版信息

JAMA Ophthalmol. 2013 Jul;131(7):898-902. doi: 10.1001/jamaophthalmol.2013.65.

Abstract

IMPORTANCE

Optic nerve hypoplasia (ONH) is an increasingly recognized cause of congenital blindness in children; however, there is significant discord regarding its incidence and the rate of associated conditions.

OBJECTIVE

To determine the incidence of ONH and the rate of associated endocrine, neurologic, and developmental abnormalities among a population-based cohort of pediatric patients.

DESIGN

Retrospective, population-based study.

SETTING

Olmsted County, Minnesota (95.7% white in 1990).

PARTICIPANTS

All pediatric residents (aged <19 years) of Olmstead County, diagnosed as having ONH from January 1, 1984, through December 31, 2008.

MAIN OUTCOMES AND MEASURES

Incidence of ONH and the rate of associated endocrine, neurologic, and developmental abnormalities.

RESULTS

Optic nerve hypoplasia was diagnosed in 19 pediatric patients during the 25-year study period, for an annual incidence of 2.4 (95% CI, 1.2-3.5) per 100,000 residents younger than 19 years or 1 in 2287 live births. The mean age at diagnosis was 2.1 years, and 10 (53%) patients were male. Commonly associated perinatal conditions included primiparity in 8 patients (42%), premature birth in 6 (32%), and maternal diabetes mellitus in 3 (16%). Of the 19 study patients, 16 (84%) had bilateral involvement at initial examination, 9 (47%) had decreased visual acuity, 8 (42%) had strabismus, and 5 (26%) had nystagmus. Systemic conditions included developmental delay in 12 (63%), neurologic deficits in 10 (53%), and endocrine dysfunction in 5 (26%).

CONCLUSIONS AND RELEVANCE

This population-based study demonstrated an incidence of ONH of 1 in 2287 live births. More than half of the patients had developmental and neurologic deficits, and one-fourth had a diagnosis of endocrine dysfunction.

摘要

重要性

视神经发育不良(ONH)是儿童先天性失明的一种日益被认识的原因;然而,其发病率和相关疾病的发生率存在很大差异。

目的

在一个基于人群的儿科患者队列中,确定 ONH 的发病率以及伴发内分泌、神经和发育异常的发生率。

设计

回顾性、基于人群的研究。

设置

明尼苏达州奥姆斯特德县(1990 年白人占 95.7%)。

参与者

奥姆斯特德县所有儿科住院医师(年龄<19 岁),1984 年 1 月 1 日至 2008 年 12 月 31 日期间被诊断为患有 ONH。

主要结果和措施

ONH 的发病率以及伴发内分泌、神经和发育异常的发生率。

结果

在 25 年的研究期间,19 名儿科患者被诊断为视神经发育不良,每年发病率为每 100000 名年龄小于 19 岁的居民中 2.4 例(95%置信区间,1.2-3.5)或每 2287 例活产儿中有 1 例。诊断时的平均年龄为 2.1 岁,10 名(53%)患者为男性。常见的围产期相关疾病包括 8 例(42%)初产妇、6 例(32%)早产和 3 例(16%)母亲糖尿病。19 名研究患者中,16 名(84%)在初次检查时双侧受累,9 名(47%)视力下降,8 名(42%)斜视,5 名(26%)眼球震颤。全身疾病包括 12 名(63%)发育迟缓、10 名(53%)神经功能缺损和 5 名(26%)内分泌功能障碍。

结论和相关性

这项基于人群的研究表明,ONH 的发病率为每 2287 例活产儿中有 1 例。超过一半的患者有发育和神经功能缺损,四分之一的患者被诊断为内分泌功能障碍。

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