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Clinical presentation of familial exudative vitreoretinopathy.

机译:家族性渗出性玻璃体视网膜病变的临床表现。

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摘要

OBJECTIVE: To describe the clinical characteristics, staging and presentation of patients with familial exudative vitreoretinopathy (FEVR) in our clinical practice over the last 25 years. DESIGN: Case series, retrospective review. PARTICIPANTS: We included 273 eyes of 145 patients. METHODS: Data collected from charts included gender, gestational age at birth, birthweight, age at presentation, referring diagnosis, family history, prior ocular surgery, and clinical presentation in each eye. Eyes with invasive posterior segment procedures before initial presentation were excluded. MAIN OUTCOME MEASURES: Demographics on presentation and clinical staging. RESULTS: Patients were slightly male predominant (57%) with a mean birthweight of 2.80 kg (range, 740 g-4.76 kg), mean gestational age of 37.8 weeks (range, 25-42), and mean age at presentation of almost 6 years (range, <1 month-49 years). A positive family history of FEVR was obtained in 18% of patients. A positive family history for ocular disease consistent with but not diagnosed as FEVR was obtained in an additional 19%. Stage 1 FEVR was identified in 45 eyes, stage 2 in 33 eyes, stage 3 in 42 eyes, stage 4 in 89 eyes, and stage 5 in 44 eyes. Radial retinal folds were seen in 77 eyes, 64 of which were temporal or inferotemporal in location. CONCLUSIONS: The FEVR patient population is remarkable for the wide range of age at presentation, gestational age, and birthweight. Although a positive family history on presentation may support the diagnosis of FEVR, a negative family history is of little help. The majority of retinal folds extended radially in the temporal quadrants, but radial folds were seen in almost all quadrants. Fellow eyes demonstrated a wide variation in symmetry. The presentation of FEVR may mimic the presentation of other pediatric and adult vitreoretinal disorders, and careful examination is often crucial in making the diagnosis of FEVR. FINANCIAL DISCLOSURE(S): The authors have no proprietary or commercial interest in any of the materials discussed in this article.
机译:目的:描述我们过去25年来临床实践中家族性渗出性玻璃体视网膜病变(FEVR)患者的临床特征,分期和表现。设计:案例系列,回顾性回顾。参与者:我们纳入了145例患者的273眼。方法:从图表中收集的数据包括性别,出生时的胎龄,出生体重,出现时的年龄,参考诊断,家族史,先前的眼科手术以及每只眼睛的临床表现。排除在初次就诊前采用有创后路手术的眼睛。主要观察指标:就诊和临床分期的人口统计学资料。结果:患者以男性为主(57%),平均出生体重为2.80 kg(范围:740 g-4.76 kg),平均胎龄为37.8周(范围:25-42),平均出现年龄为6岁年(范围,<1个月-49年)。 18%的患者获得了FEVR的阳性家族史。另有19%的人获得了与但未诊断为FEVR的阳性眼病家族史。 FEVR分为1阶段45眼,2阶段33眼,3阶段42眼,4阶段89眼,5阶段44眼。在77只眼中可见骨视网膜褶皱,其中64只在颞部或颞下颞部。结论:FEVR患者人群在表现年龄,胎龄和出生体重方面具有广泛的意义。尽管呈报阳性的家族史可以支持FEVR的诊断,但是阴性家族史几乎没有帮助。大部分视网膜褶皱在颞象限中呈放射状延伸,但几乎在所有象限中都可见到放射状褶皱。同胞的眼睛表现出很大的对称性差异。 FEVR的表现可能模仿其他小儿和成人玻璃体视网膜疾病的表现,仔细检查通常对于诊断FEVR至关重要。财务披露:作者对本文讨论的任何材料均没有所有权或商业利益。

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