purpose : to evaluate the efficacy of autologous plasmin in pediatric vitrectomy and to report the anatomic outcomes of autologous plasmin assisted pediatric vitrectomy methods : in an interventional prospective study, thirty-four pediatric patients with vitreoretinal disorders who needed vitrectomy during 2008 to 2010, included in the study. the patients were divided into two groups: the retin...

purpose: to evaluate the clinical features, and functional and anatomical outcomes of surgical intervention for pediatric rhegmatogenous retinal detachment (rrd). methods: in this retrospective case series, pediatric patients with rrd who had undergone surgical intervention were included. cases were categorized into five main etiological groups: congenital or developmental (48 eyes), traumatic ...

Purpose: To evaluate the efficacy of autologous plasmin in pediatric vitrectomy and to report the anatomic outcomes of autologous plasmin assisted pediatric vitrectomy Methods: In an interventional prospective study, Thirty-four pediatric patients with vitreoretinal disorders who needed vitrectomy during 2008 to 2010, included in the study. The patients were divided into two groups: the retinop...

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Since the first vitrectomy surgery was used for treatment of vitreoretinal diseases, surgical techniques and instrumentation have been rapidly improved in the past decades. However, there are complicated vitreoretinal diseases that cannot be successfully treated, even with state-of-the-art surgeries. The outcomes of some complicated cases are still poor due to different reasons and debates stil...

type transthyretin as well as other fibrillar proteins. To our knowledge, this is the first case report of vitreoretinal amyloidosis in the absence of transthyretin mutations. In addition, no signs of systemic amyloidosis suggestive of FAP were evident 7 years after the patient’s initial presentation, although we cannot exclude the possibility of a subclinical level of amyloid deposition in oth...

Incontinentia pigmenti is a very rare X-linked dominant inherited disease characterized by skin lesions, retinal pathologies, central nervous system anomalies, and dental problems. Norrie recessive severe vitreoretinal dysplasia in both eyes at birth. In diseases, patients can apply to the clinic with nystagmus, leukocoria, microphthalmia, detachment an early age. this review, disease, which ar...