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Juvenile Macular Degenerations

机译:少年黄斑退化

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摘要

In this article, we review the following 3 common juvenile macular degenerations: Stargardt disease, X-linked retinoschisis, and Best vitelliform macular dystrophy. These are inherited disorders that typically present during childhood, when vision is still developing. They are sufficiently common that they should be included in the differential diagnosis of visual loss in pediatric patients. Diagnosis is secured by a combination of clinical findings, optical coherence tomography imaging, and genetic testing. Early diagnosis promotes optimal management. Although there is currently no definitive cure for these conditions, therapeutic modalities under investigation include pharmacologic treatment, gene therapy, and stem cell transplantation.
机译:在本文中,我们审查以下3个常见的青少年黄斑退化:Stargardt疾病,X-Linked Retinoschisis,以及最佳的vitelliform黄斑营养不良症。 当视力仍在开发时,这些是通常在童年期间存在的遗传障碍。 它们足以很常见,它们应该被纳入儿科患者视力损失的差异诊断。 通过临床发现,光学相干断层扫描成像和遗传测试的组合来确保诊断。 早期诊断促进最佳管理。 虽然目前没有确定这些条件的固化,但调查的治疗方式包括药理学治疗,基因治疗和干细胞移植。

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