Ocular findings of elderly cases of homozygous sickle-cell disease in Jamaica.

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منابع مشابه

Ocular findings of elderly cases of homozygous sickle-cell disease in Jamaica.

The ocular fingings in 60 patients with homozygous sickle-cell disease over the age of 40 years have been described. Peripheral retinal vessel disease was common and appeared to increase with age. Retinitis proliferans was common among older patients in the group. Angioid streaks occurred in 13 (22 per cent) patients.

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Ocular findings in children with sickle cell haemoglobin C disease in Jamaica.

The development of severe retinal vascular disease and retinitis proliferans in sickle cell haemoglobin C disease (SC disease) is well recognized (Welch and Goldberg, I966; Goldberg, 197I; Condon and Serjeant, I972a). In a recent survey in Jamaica, Condon and Serjeant (1972a) noted retinitis proliferans in 23 (33 per cent.) of seventy adults with SC disease. The changes were found in some patie...

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Subjective well-being of adults with homozygous sickle cell disease in Jamaica.

OBJECTIVES This study compared the subjective well-being of adults with homozygous sickle cell (SS) disease to a matched group of healthy adult peers. The differential influence of sociodemographic factors on the subjective well-being of Sickle Cell patients was also examined. METHODS The Ferran and Powers Quality of Life Index and the Positive and Negative Affect Schedule were used to assess...

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Sickle cell-thalassemia disease in Jamaica.

SICKLE CELL-thalassemia disease was first reported by Silvestroni and Bianco in Italians in Europe.13 Cases have also been described in Italians and Greeks in the United States,48 in Negroes in Africa9 and the United States1013 and in Eti-Turks.’4 A recent paper describes 44 cases of the disease in Greece.3#{176} Sickle cell-thalassemia disease results from the inheritance of two genes, the sic...

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Ocular findings in Saudi Arabian patients with sickle cell disease.

AIM This study was set up to determine whether or not retinal changes occur in sickle cell disease in Saudi Arabian subjects with either the Benin, which exists in the south western part of the kingdom, or Asian haplotypes in the east, and to compare the findings with those in sickle cell disease in Jamaica. METHODS Retinal examination and fluorescein angiography were performed in 61 patients...

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ژورنال

عنوان ژورنال: British Journal of Ophthalmology

سال: 1976

ISSN: 0007-1161

DOI: 10.1136/bjo.60.5.361