Ocular Cases

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Ocular Oncology Cases from Cole

SEPTEMBER 2010 ADVANCED OCULAR CARE 31 CASE PRESENTATION A 76-year-old white man was referred to our clinic for evaluation of a pigmented lesion that recently increased in size. He had first noticed the abnormal iris pigmentation of his right eye 20 years ago and had been under observation for the previous 5 years. The patient denied any ocular or systemic symptoms; his past medical history was...

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Ocular cases of medical interest.

Case Reports Case 1. Myopathica Atrophica.-A yeoman of signals aged 22 years was admitted to the Military Hospital, Gibraltar, on August 31, 1943. He complained of having difficulty in facing the light for 10 days. The eyes ached -but did not water, and had become bloodshot in the last 2 months, but especially in the last week when he attended the American hospital at Londonderry for conjunctiv...

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Ocular Tumors In Iran: A 10-Year Histopathological Study On 384 Cases Of Enucleation

  Background and Objective: The frequency and pattern of eye neoplasms differ in various geographic areas. Our aim was to determine the distribution of patient age, gender, ocular tumor origin, location and histological type in our region. Materials and Methods: In this cross-sectional study, all of the 384 eye globe enucleation cases carried out during a 10-year period in Farabi Medical Cent...

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Frequency of ocular involvement in 100 cases of Behcet syndrome in Babol, North of Iran

Background: Behcet syndrome is a recurrent inflammatory disorder that frequently involves the ocular system. The purpose of this study was to determine the frequency of ocular involvement in cases of Behcet's disease in Babol, north of Iran. Methods: From April 2003 to December 2009, 100 cases of behcet's disease who were admitted at the Department of Ophthalmology and Internal Medicine of Babo...

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11p13 deletion, Wilms' tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases.

Three cases of Wilms' tumour and sporadic aniridia were followed up for periods ranging from 32 months to seven years. All had a deletion of the short arm of the eleventh chromosome 11p13, including one case with mosaicism, a cytogenetic feature that has not been previously described in the Wilms' tumour and sporadic aniridia association. Unusual non-ocular features found in all patients includ...

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ژورنال

عنوان ژورنال: BMJ

سال: 1876

ISSN: 0959-8138,1468-5833

DOI: 10.1136/bmj.1.806.720-a