Optic disc anomalies

视盘异常
  • 文章类型: Journal Article
    先天性肾脏和泌尿道异常(CAKUT)是全球最常见的出生缺陷之一,也是儿童肾衰竭的主要原因。肾外表现也很常见。这项研究回顾了与基因组学英格兰CAKUT相关基因小组相关的眼部异常疾病。此外,使用人类蛋白质图谱和小鼠基因组信息学数据库检查每个基因在人类视网膜中的表达和小鼠模型中的眼部表型,分别。63个CAKUT相关基因中有34个(54%)(55个“绿色”和8个“琥珀色”)具有已报告的眼部表型。6个最常见的CAKUT相关基因中的5个(PAX2,EYA1,SALL1,GATA3,PBX1)代表所有诊断的30%具有眼部特征。与大多数CAKUT相关基因和六个最常见基因中的五个发现的眼部异常是结肠瘤,小眼症,视盘异常,屈光误差(散光,近视,和远视),和白内障。研究的CAKUT相关基因中有7个(11%)没有报道的眼部特征,但在人类视网膜中表达或在小鼠模型中具有眼部表型。这表明了进一步可能无法识别的异常。约三分之一的CAKUT相关基因(18,29%)没有眼部关联,并且在视网膜中没有表达,相应的小鼠模型没有眼部表型。CAKUT患者的眼部异常提示该疾病的遗传基础,有时提示受影响的基因。患有CAKUT的人通常有眼部异常,可能需要进行眼科检查,监测,和保持视力的治疗。
    Congenital anomalies of the kidney and urinary tract (CAKUT) are among the most common birth defects worldwide and a major cause of kidney failure in children. Extra-renal manifestations are also common. This study reviewed diseases associated with the Genomics England CAKUT-associated gene panel for ocular anomalies. In addition, each gene was examined for expression in the human retina and an ocular phenotype in mouse models using the Human Protein Atlas and Mouse Genome Informatics databases, respectively. Thirty-four (54%) of the 63 CAKUT-associated genes (55 \'green\' and 8 \'amber\') had a reported ocular phenotype. Five of the 6 most common CAKUT-associated genes (PAX2, EYA1, SALL1, GATA3, PBX1) that represent 30% of all diagnoses had ocular features. The ocular abnormalities found with most CAKUT-associated genes and with five of the six commonest were coloboma, microphthalmia, optic disc anomalies, refraction errors (astigmatism, myopia, and hypermetropia), and cataract. Seven of the CAKUT-associated genes studied (11%) had no reported ocular features but were expressed in the human retina or had an ocular phenotype in a mouse model, which suggested further possibly-unrecognised abnormalities. About one third of CAKUT-associated genes (18, 29%) had no ocular associations and were not expressed in the retina, and the corresponding mouse models had no ocular phenotype. Ocular abnormalities in individuals with CAKUT suggest a genetic basis for the disease and sometimes indicate the affected gene. Individuals with CAKUT often have ocular abnormalities and may require an ophthalmic review, monitoring, and treatment to preserve vision.
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  • 文章类型: Journal Article
    视盘异常包括,有髓神经纤维,视盘玻璃疣,和Bergmeister乳头.使用光学相干断层扫描-血管造影(OCTA)对视盘异常中的放射状乳头周围毛细血管(RPC)网络进行成像,可以在这些条件下提供有关RPC网络的信息。
    该视频描述了在视盘异常且椎间盘表面有异常组织的情况下,使用血管椎间盘模式的视神经头和RPC网络的OCTA。
    本视频展示了有髓鞘神经纤维一只眼睛内RPC网络的特征,视盘玻璃疣,和Bergmeister乳头.
    OCTA在具有椎间盘表面异常组织的视盘异常中显示出密集的RPC微血管网。OCTA是研究血管丛/RPC及其在这些椎间盘异常中的改变的有效成像方式。
    https://youtu。是/zlflgijy56c。
    Optic disc anomalies with abnormal tissue on the disc surface includes, myelinated nerve fiber, optic disc drusen, and Bergmeister papillae. Imaging the radial peripapillary capillary (RPC) network in optic disc anomalies with optical coherence tomography-angiography (OCTA) can give information on the RPC network in these conditions.
    This video describes the OCTA of optic nerve head and RPC network using the angio disc mode in cases of optic disc anomalies with abnormal tissue on the disc surface.
    This video presents characteristic features of RPC network in one eye each of myelinated nerve fiber, optic disc drusen, and Bergmeister papillae.
    OCTA in optic disc anomalies with abnormal tissue on the disc surface show a dense RPC microvascular network. OCTA is an effective imaging modality to study vascular plexus/RPC and their alteration in these disc anomalies.
    https://youtu.be/zlflgijy56c.
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  • 文章类型: Journal Article
    目的:这项研究的目的是调查土耳其先天性视盘异常的患病率。
    方法:对5570例患者的11,123只眼进行视盘异常筛查。所有患者均接受完整的眼科检查,包括最佳矫正视力,折射,球形当量,裂隙灯生物显微镜,眼内压测量,扩张立体眼底检查。数据分析使用SPSSforWindows进行,版本22.0(SPSSInc.,芝加哥,IL,美国)。
    结果:对5570名参与者的11,123只眼进行了筛查。在5570名接受视盘检查的参与者中,174例患者的246只眼(3.12%,95%CI=2.66-3.58%)有视盘畸形。92人(52.9%)为女性,82(47.1%)为男性,平均年龄为44.25±15.67岁。72例(41.4%)患者为双侧,102例(58.6%)患者单侧受累。椎间盘倾斜是最常见的异常,在46例患者(75只眼)和所有筛查患者中发现至少一只眼睛。乳头周围有髓神经纤维是第二个常见异常,在31名受试者(35只眼)和所有筛查受试者的0.56%中发现至少一只眼睛。乳头状周围萎缩是第三个常见的异常,并且在24例患者(37只眼)和所有筛选对象的0.43%中至少有一只眼睛被发现。
    结论:据我们所知,这是土耳其所有先天性视盘异常患病率的第一项研究。先天性视盘异常的患病率高于其他国家。
    OBJECTIVE: The aim of this study was to investigate the prevalence of congenital optic disc anomalies in Turkey.
    METHODS: The 11,123 eyes of 5570 patients were screened for optic disc anomalies. All patients were underwent a complete ophthalmic examination including best corrected visual acuity, refraction, spherical equivalent, slit lamp biomicroscopy, intraocular pressure measurements, dilated stereoscopic fundus examination. Data analyses were performed by using SPSS for Windows, version 22.0 (SPSS Inc., Chicago, IL, United States).
    RESULTS: 11,123 eyes of 5570 participants were screened. Of the 5570 participants who underwent optic disc examination, 246 eyes of 174 patients (3.12%, 95% CIs 2.66-3.58%) had optic disc anormalies. 92 (52.9%) were female, 82 (47.1%) were male and the mean of age was 44.25 ± 15.67 years. 72 (41.4%) patients were bilateral, 102 (58.6%) patients were unilateral involvement. The tilted disc was the most common anomaly and was found at least one eye in 46 patients (75 eyes) and 0.83% of all screened patients. Peripapillary myelinated nerve fibers was the second common anomaly and was found at least one eye in 31 subjects (35 eyes) and 0.56% of all screened subjects. Peripapillary atrophy was the third common anomaly, and was found in at least one eye in 24 patients (37 eyes) and 0.43% of all screened subjects.
    CONCLUSIONS: To our knowledge, this is the first study that the prevalences of all congenital optic disc anomalies from Turkey. The prevalence of congenital optic disc anomalies is higher than in other countries.
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