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Macular hypoplasia (or foveal hypoplasia) is a rare medical condition involving the underdevelopment of the macula, [1] a small area on the retina (the eye's internal surface) responsible for seeing in detail and sensing light. [2] Macular hypoplasia is often associated with albinism. [1]
The macula (/ˈmakjʊlə/) [1] or macula lutea is an oval-shaped pigmented area in the center of the retina of the human eye and in other animals. The macula in humans has a diameter of around 5.5 mm (0.22 in) and is subdivided into the umbo , foveola , foveal avascular zone , fovea , parafovea , and perifovea areas.
The area of the macula constitutes only about 2.1% of the retina, and the remaining 97.9% (the peripheral field) remains unaffected by the disease. Even though the macula provides such a small fraction of the visual field, almost half of the visual cortex is devoted to processing macular information. [14]
The onset of symptoms and the severity of vision loss vary widely. The adult-onset form begins later, usually in middle age, and tends to cause relatively mild vision loss. The two forms of vitelliform macular dystrophy each have characteristic changes in the macula that can be detected during an eye examination.
The foveola is located within a region called the macula, a yellowish, cone photoreceptor filled portion of the human retina. Approximately 0.35 mm in diameter, the foveola lies in the center of the fovea and contains only cone cells and a cone-shaped zone of Müller cells. [1]
It is a diagnostic tool that aids in the detection of visual disturbances caused by changes in the retina, particularly the macula (e.g. macular degeneration, Epiretinal membrane), as well as the optic nerve and the visual pathway to the brain.
Diagram of the human eye showing macula and fovea. Although J. D. Gass originally identified four types of idiopathic juxtafoveolar retinal telangiectasis in 1982, contemporary researchers describe three types collectively known as idiopathic juxtafoveal telangiectasia: macular telangiectasia type 1, macular telangiectasia type 2, and macular telangiectasia type 3.
The foveal avascular zone (FAZ) is a region within the fovea centralis at the centre of the retina of the human eye that is devoid of retinal blood vessels. The geometric centre of the FAZ is often taken to be the centre of the macula and thus the point of fixation. [1] The FAZ is an important anatomical landmark in fluorescein angiography.