1) Proliferative Diabetic Retinopathy
增生性糖尿病性视网膜病变
1.
Clinical Application of Fiberoptic-Free Bimanual Vitrectomy with A Novel System in Proliferative Diabetic Retinopathy;
无光导-双手法玻璃体切割术在增生性糖尿病性视网膜病变中的应用
2.
Vitrectomy combined with phacoemulsification for proliferative diabetic retinopathy
玻璃体切除术联合晶状体手术治疗增生性糖尿病性视网膜病变
2) proliferative diabetic retinopathy
增生性糖尿病视网膜病
1.
Pars plana vitrectomy combined with phacoemulsification and intraocular lens implantation for proliferative diabetic retinopathy;
玻璃体切割联合超声乳化人工晶体植入术治疗增生性糖尿病视网膜病变
3) proliferative diabetic retinopathy
增生性糖尿病视网膜病变
1.
Different intraocular tamponade during vitrectomy on proliferative diabetic retinopathy;
增生性糖尿病视网膜病变患者玻璃体手术不同眼内填充物的效果分析
2.
Expression of MMP-2 and MMP-9 in vitrectomy specimens with proliferative diabetic retinopathy;
增生性糖尿病视网膜病变玻璃体切除物中MMP-2和MMP-9的表达
3.
Surgical treatment of proliferative diabetic retinopathy.;
增生性糖尿病视网膜病变的手术治疗观察
4) proliferative diabetic retinopathy(PDR)
增生型糖尿病[性]视网膜病变
5) PDR
增殖性糖尿病性视网膜病变
1.
Objective:To explore the effect and the filling material of vitrectomy combining with laser on the treatment of PDR.
目的:观察分析玻璃体切割联合激光治疗增殖性糖尿病性视网膜病变的疗效及充填材料选择。
2.
Objective:To assess the incidence of apoptosis in epiretinal membranes from eyes with proliferative vitreoretinopathy(PVR),proliferative diabetic retinopathy (PDR),and macular pucker (MP) and to further investigate the potential involvement of key executors of apoptosis.
方法 :2 3例增殖性玻璃体视网膜病变 (PVR) ,增殖性糖尿病性视网膜病变 (PDR) ,黄斑裂孔 (MH)及黄斑前膜 (MP)的视网膜前膜 (epiretinalmem brane,ERM )由玻璃体切割术中取得。
6) Proliferative diabetic retinopathy
增生性糖尿病性视网膜病
1.
AIM:To investigate patient assessed visual function and visual acuity after treatment with the unselective anti-VEGF inhibitor bevacizumab in diabetic macular edema after scatter laser photocoagulation due to proliferative diabetic retinopathy(PDR) .
目的:增生性糖尿病性视网膜病播散性视网膜激光光凝后,用非选择性抗VEGF抑制剂贝伐单抗治疗糖尿病性黄斑水肿,调查患者自我评估的视功能及视力。
补充资料：性幼稚-色素性视网膜炎-多指畸形综合征
性幼稚-色素性视网膜炎-多指畸形综合征
病名。亦称劳-穆-比综合征。其临床特点为肥胖、性腺发育不良、智力低下、色素性视网膜炎、多指或并指畸形以及其他先天性异常等。 早在1866年由Laurence等首先报道。其性腺发育不良表现为阴茎小、睾丸不发育、 外生殖器呈幼稚型、阴囊有时分裂，以及青春期不出现第二性征等。部分可出现各 种类型先天性心脏病、肾脏的先天异常、神经系统的先天异常、骨骼系统的先天 性异常，以及颜面的先天性异常等。血、尿中促性腺激素明显降低，睾酮亦明显低下 ，尿中17-酮类固醇含量亦低于正常。睾丸活检可见曲细精管结构基本正常，但缺乏精子形成。间质细胞亦未见异常改变。多有阳性家族史，染色体组型正常。属常染色体隐性遗传性疾病。无特殊治疗方法。针对睾丸功能低下可进行性激素治疗。
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参考词条