Ocular infections with helminthic parasites are uncommon and have been well described previously.

的寄生虫感染相当少见，但陆续都有病例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力的病均以白内障居首位，其次为角膜病、光、底病等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小球是一种先天发育异常性疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无球外伤病史，且检查均无虹膜新生血管、幼年型黄色肉芽肿或者疱疹病毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通常发生在女性，除了皮肤以外还可能出现，牙齿，骨骼，以及中枢神经系统的异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目的研究兔角膜穿孔伤后血-屏障的改变及川芎嗪对环丙沙星在兔角膜穿孔伤内渗透性的影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

球外肌是维持球正常运动及形成正常视觉的关键因素,其病变表现为斜视及球运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

眼睛的寄生虫感染相当少见，但陆续都有例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力的眼均以白内障居首位，其次为角膜、光眼、眼底等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无眼球外伤史，且眼科学检查均无虹膜新生血管、幼年型黄色肉芽肿或者毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾，通常发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目的研究兔角膜穿孔伤后血-眼屏障的改变及川芎嗪对环丙沙星在兔眼角膜穿孔伤眼内渗透性的影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

眼球外肌是维持眼球正常运动及形成正常视觉的关键因素,其变表现为斜视及眼球运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

睛的寄生虫感染相当少见，但陆续都有病例被报。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

和低视力的病均以白内障居首位，其次为角膜病、光、底病等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小球是一种先天发育异常性病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无球外伤病史，且学检查均无虹膜新生血管、幼年型黄色肉芽肿或者疱疹病毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传病，通常发生在女性，除了皮肤以外还可能出现睛，牙齿，骨骼，以及中枢神经系统的异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目的研究兔角膜穿孔伤后血-屏障的改变及川芎嗪对环丙沙星在兔角膜穿孔伤内渗透性的影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

球外肌是维持球正常运动及形成正常视觉的关键因素,其病变表现为斜视及球运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

眼睛的寄生虫感染相当少见，但陆续都有病例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力的眼病均以白内障居首位，其次为角膜病、光眼、眼底病。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育性眼科疾病,遗传方式有染色体显性遗传、染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无眼球外伤病史，且眼科学检查均无虹膜新生血管、幼年型黄色肉芽肿或者疱疹病毒感染发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通发生在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩膜伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目的研究兔角膜穿孔伤后血-眼屏障的改变及川芎嗪对环丙沙星在兔眼角膜穿孔伤眼内渗透性的影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

眼球外肌是维持眼球正运动及形成正视觉的关键因素,其病变表现为斜视及眼球运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

眼睛寄生虫感染相当少见，但陆续都有例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力眼均以白内障居首位，其次为角、光眼、眼底等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无眼球史，且眼科学检查均无虹新生血管、幼年型黄色肉芽肿或者疱疹毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤遗传疾，通常发生在女性，除了皮肤以还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通角巩口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通角巩口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目研究兔角穿孔后血-眼屏障改变及川芎嗪对环丙沙星在兔眼角穿孔眼内渗透性影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

眼球肌是维持眼球正常运动及形成正常视觉关键因素,其变表现为斜视及眼球运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

眼寄生虫感染相当少见，但陆续都有病例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力眼病均以白内障居首位，其次为角膜病、光眼、眼底病等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科病,方式有常染色体显性、常染色体隐性和X连锁隐性。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无眼球外伤病史，且眼科学检查均无虹膜新生血管、幼年型黄色肉芽肿或者疱疹病毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤病，通常发生在女性，除了皮肤以外还可能出现眼，牙齿，骨骼，以及中枢神经系统异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩膜伤口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩膜伤口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目研究兔角膜穿孔伤后血-眼屏障改变及川芎嗪对环丙沙星在兔眼角膜穿孔伤眼内渗透性影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

眼球外肌是维持眼球正常运动及形成正常视觉关键因素,其病变表现为斜视及眼球运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

眼睛的寄虫感染相当少见，但陆续都有病例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力的眼病均以白内障居首位，其次为角病、眼、眼底病等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无眼球外伤病史，且眼科学检查均无虹血管、幼年型黄色肉芽肿或者疱疹病毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见的皮肤遗传疾病，通常发在女性，除了皮肤以外还可能出现眼睛，牙齿，骨骼，以及中枢神经系统的异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼球穿通伤角巩伤口修补的同时行超声乳化白内障吸除加后房型人工晶体植入手术的效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目的研究兔角穿孔伤后血-眼屏障的改变及川芎嗪对环丙沙星在兔眼角穿孔伤眼内渗透性的影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

眼球外肌是维持眼球正常运动及形成正常视觉的关键因素,其病变表现为斜视及眼球运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

眼睛寄生虫感染相当少见，但陆续都有病例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力眼病均以白内障居首位，其次为角病、光眼、眼底病等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小眼是一种先天发育异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无眼病史，且眼科学检查均无虹新生血管、幼年型黄色肉芽肿或者疱疹病毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤遗传疾病，通常发生在女性，除了皮肤以还可能出现眼睛，牙齿，骨骼，以及中枢神经系统异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼穿通角巩口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨眼穿通角巩口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目研究兔角穿孔后血-眼屏障改变及川芎嗪对环丙沙星在兔眼角穿孔眼内渗透性影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

眼肌是维持眼正常运动及形成正常视觉关键因素,其病变表现为斜视及眼运动障碍。

Ocular infections with helminthic parasites are uncommon and have been well described previously.

睛寄生虫感染相当少见，但陆续都有病例被报告。

The causes leading to blindness and low vision were cataract, ceratonosus, glaucoma and ocular fundus Disease, etc.

致盲和致低视力病均以白内障居首位，其次为角膜病、光、底病等。

Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance.

先天性小是一种先天发育异常性科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。

No trauma history could be elicited.Ocular examinations revealed no pertinent findings, such as rubeosis irides, juvenile xanthogranuloma, or Herpes infections.

两例均无伤病史，且科学检查均无虹膜新生血管、幼年型黄色肉芽肿或者疱疹病毒感染等异常发现。

Incontinentia pigmenti is a rare genodermatosis that usually affects female infants.The associated abnormalities involve ocular, dental, skeletal and central nervous systems.

色素失禁症是一种罕见皮肤遗传疾病，通常发生在女性，除了皮肤以还可能出现睛，牙齿，骨骼，以及中枢神经系统异常。

To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨穿通伤角巩膜伤口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective:To investigate the effect of corneosclera repair and ultrasonic emulsification and cataract aspiration followed by artificial vitreous implantation in ocular penetrating injury.

探讨穿通伤角巩膜伤口修补同时行超声乳化白内障吸除加后房型人工晶体植入手术效果。

Objective To investigate the changes of blood-ocular barrier and effect of ligustrazine on the ocular endosmosis of intravenous ciprofloxacin in rabbit eyes of corneal perforating injury.

目研究兔角膜穿孔伤后血-屏障改变及川芎嗪对环丙沙星在兔角膜穿孔伤内渗透性影响。

Extraocular muscles play an important role in the normal movement of globe and formation of normal vision,whose lesions may result in strabism and ocular motor disturbance.

肌是维持正常运动及形成正常视觉关键因素,其病变表现为斜视及运动障碍。