Stargardt macular degeneration
Última actualización 27 Oct 2023
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Stargardt macular degeneration is a genetic eye disorder that causes progressive vision loss. This disorder affects the retina, the specialized light-sensitive tissue that lines the back of the eye. Specifically, Stargardt macular degeneration affects a small area near the center of the retina called the macula. The macula is responsible for the type of vision needed for detailed tasks such as reading, driving, and recognizing faces. In most people with Stargardt macular degeneration, a fatty yellow pigment called lipofuscin builds up in cells underlying the macula. Over time, the abnormal accumulation of this substance can damage cells that are critical for clear vision. People with Stargardt macular degeneration have problems with night vision that can make it difficult to navigate in low light. Some affected individuals also have impaired colour vision. The signs and symptoms of Stargardt macular degeneration typically appear in late childhood to early adulthood and worsen over time.
Descripción
Stargardt macular degeneration is a genetic eye disorder that causes progressive vision loss. This disorder affects the retina, the specialized light-sensitive tissue that lines the back of the eye. Specifically, Stargardt macular degeneration affects a small area near the center of the retina called the macula. The macula is responsible for the type of vision needed for detailed tasks such as reading, driving, and recognizing faces. In most people with Stargardt macular degeneration, a fatty yellow pigment called lipofuscin builds up in cells underlying the macula. Over time, the abnormal accumulation of this substance can damage cells that are critical for clear vision. People with Stargardt macular degeneration have problems with night vision that can make it difficult to navigate in low light. Some affected individuals also have impaired colour vision. The signs and symptoms of Stargardt macular degeneration typically appear in late childhood to early adulthood and worsen over time.
Patrones de herencia
The source lists the following possible inheritance patterns: Autosomal recessive; Autosomal dominant. More than one pattern can apply in different cases.
Related genes
Otros nombres
Juvenile macular degeneration
Macular dystrophy with flecks, type 1
Stargardt disease
STGD
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Problemas visuales
Opticians can d... See the separate leaflet called Chronic open-angle glaucoma for more details. Degeneración macular (MD) The mácula es the spot on the back of the eye cuál sees the things that are looked at directly. Macular degeneration occurs when esto area of the retina degenerates and loses function. This results in gradual loss of central.

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Problemas oculares
Consulte el folleto separado llamado Desprendimiento de retina. Degeneración macular El mácula is the small area of the retina at the back of your eye and responsible for your central vision. Degeneración macular relacionada con la edad (AMD, or ARMD) is the most common cause of severe sight problems in the developed world. It causes a gradual loss of central vision..

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Cataratas
For some people, the cataract never becomes bad enough to impair vision. Two of the most important are macular degeneration and glaucoma. Symptoms of macular degeneration Macular degeneration is also mainly asociado con getting older. It affects the central part of your vision. However, protecting your eyes from UV light, eating a healthy diet.

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Prevención de caídas en personas mayores
A disorder of the brain ( Wernicke-Korsakoff syndrome ) can also cause falls. Problems with visión : for example, clouding of the lens of el eye ( catarata ) y visual field defects , where part de the field of vision appears to be missing. Breakdown of el cells lining el back of el eye is known as age-related macular degeneration. It is a.

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Envejecimiento
Ageing (also spelt aging) is the process of becoming older. This happens continually throughout life. Older age tends to bring with it unwelcome changes such as a greater risk of health problems and typical changes to appearance. Changes to hair colour (grey/white) and pattern (balding, particularly in men). Deterioration in memory. Deterioration.
Lecturas adicionales y referencias
- Stargardt macular degeneration; MedlinePlus, National Library of Medicine.
- Molday RS, Zhang K. Defective lipid transport and biosynthesis in recessive and dominant Stargardt macular degeneration. Prog Lipid Res. 2010 Oct;49(4):476-92. doi: 10.1016/j.plipres.2010.07.002. Epub 2010 Jul 13.
- Molday RS, Zhong M, Quazi F. The role of the photoreceptor ABC transporter ABCA4 in lipid transport and Stargardt macular degeneration. Biochim Biophys Acta. 2009 Jul;1791(7):573-83. doi: 10.1016/j.bbalip.2009.02.004. Epub 2009 Feb 20.
- Walia S, Fishman GA. Natural history of phenotypic changes in Stargardt macular dystrophy. Ophthalmic Genet. 2009 Jun;30(2):63-8. doi: 10.1080/13816810802695550.
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