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Causes of Age-related macular degeneration

List of causes of Age-related macular degeneration

Following is a list of causes or underlying conditions (see also Misdiagnosis of underlying causes of Age-related macular degeneration) that could possibly cause Age-related macular degeneration includes:

Age-related macular degeneration Causes: Book Excerpts

Age-related macular degeneration as a symptom:

Conditions listing Age-related macular degeneration as a symptom may also be potential underlying causes of Age-related macular degeneration. Our database lists the following as having Age-related macular degeneration as a symptom of that condition:

Medical news summaries relating to Age-related macular degeneration:

The following medical news items are relevant to causes of Age-related macular degeneration:

Related information on causes of Age-related macular degeneration:

As with all medical conditions, there may be many causal factors. Further relevant information on causes of Age-related macular degeneration may be found in:

Causes of Age-related macular degeneration: Online Medical Books

16 MEDICAL BOOKS ONLINE! Review excerpts from medical books online, free, without registration, for more information about the causes of Age-related macular degeneration.

Scotoma: Medical causes
(Handbook of Signs & Symptoms (Third Edition))

Chorioretinitis

Inflammation of the choroid and retina produces a paracentral scotoma. Ophthalmoscopic examination reveals clouding and cells in the vitreous, subretinal hemorrhage, and neovascularization. The patient may have photophobia along with blurred vision.

Macular degeneration

Any degenerative process or disorder affecting the fovea centralis results in a central scotoma. Ophthalmoscopic examination reveals changes in the macular area. The patient may notice subtle changes in visual acuity, in color perception, and in the size and shape of objects.

Optic neuritis

Inflammation, degeneration, or demyelination of the optic nerve produces a central, circular, or centrocecal scotoma. The scotoma may be unilateral with involvement of one nerve, or bilateral with involvement of both nerves. It can vary in size, density, and symmetry. The patient may report severe vision loss or blurring, lasting up to 3 weeks, and pain — especially with eye movement. Common ophthalmoscopic findings include hyperemia of the optic disk, retinal vein distention, blurred disk margins, and filling of the physiologic cup.

Retinal pigmentary degeneration

Retinal pigmentary degeneration causes premature retinal cell changes leading to cell death. One disorder, retinitis pigmentosa, initially involves loss of peripheral rods; the resulting annular scotoma progresses concentrically until only a central field of vision (tunnel vision) remains. The earliest symptom —  impaired night vision —  appears during adolescence. Associated signs include narrowing of the retinal blood vessels and pallor of the optic disk. Eventually, with invasion of the macula, blindness may occur.

» READ BOOK EXCERPT ONLINE »

Source: Handbook of Signs & Symptoms (Third Edition), 2006

Age-related macular degeneration: Causes and incidence
(Professional Guide to Diseases (Eighth Edition))

Age-related macular degeneration results from underlying pathologic changes that occur primarily at the level of the retinal pigment epithelium, Bruch’s membrane, and the choriocapillaris in the macular region. Drusen (bumps), which are common in elderly people, appear as yellow deposits beneath the pigment epithelium and may be prominent in the macula. No predisposing conditions have been identified; however, some forms of the disorder are hereditary.

Macular degeneration is the most common cause of legal blindness in adults, accounting for about 12% of blindness cases in the United States and for about 17% of new blindness cases. It’s also one of the causes of severe irreversible loss of central vision in elderly people — by age 75, almost 15% of people have this condition. Whites have the highest incidence. Other risk factors are family history and cigarette smoking.

» READ BOOK EXCERPT ONLINE »

Source: Professional Guide to Diseases (Eighth Edition), 2005

Scotoma: Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))

Chorioretinitis

Inflammation of the choroid and retina produces a paracentral scotoma. Ophthalmoscopic examination reveals clouding and cells in the vitreous, subretinal hemorrhage, and neovascularization. The patient may have photophobia along with blurred vision.

Glaucoma

Prolonged elevation of IOP can cause an arcuate scotoma. Poorly controlled glaucoma can also cause cupping of the optic disk, loss of peripheral vision, and reduced visual acuity. The patient may also see rainbow-colored halos around lights.

Macular degeneration

Any degenerative process or disorder affecting the fovea centralis results in a central scotoma. Ophthalmoscopic examination reveals changes in the macular area. The patient may notice subtle changes in visual acuity, in color perception, and in the size and shape of objects.

Migraine headache

Transient scintillating scotomas, usually bilateral and often homonymous, can occur during a classic migraine aura. Besides pain, characteristic associated symptoms include paresthesia of the lips, face, or hands; slight confusion; dizziness; and photophobia.

Optic neuritis

Inflammation, degeneration, or demyelination of the optic nerve produces a central, circular, or centrocecal scotoma. The scotoma may be unilateral with involvement of one nerve, or bilateral with involvement of both nerves. It can vary in size, density, and symmetry. The patient may report severe visual loss or blurring, lasting up to 3 weeks, and pain—especially with eye movement. Common ophthalmoscopic findings include hyperemia of the optic disk, retinal vein distention, blurred disk margins, and filling of the physiologic cup.

Retinal pigmentary degenerations

These disorders cause premature retinal cell changes leading to cell death. One disorder, retinitis pigmentosa, initially involves loss of peripheral rods; the resulting annular scotoma progresses concentrically until only a central field of vision (tunnel vision) remains. The earliest symptom—impaired night vision—appears during adolescence. Associated signs include narrowing of the retinal blood vessels and pallor of the optic disk. Eventually, with invasion of the macula, blindness may occur.

» READ BOOK EXCERPT ONLINE »

Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006

Retinal Phenomena: Differential Overview
(Field Guide to Bedside Diagnosis)

❑ Hypertension

❑ Diabetic retinopathy

❑ Glaucoma

❑ Cholesterol emboli

❑ Papilledema

❑ Pigmented crescent

❑ Macular degeneration

❑ Retinal detachment

❑ Acute optic neuritis

❑ Optic atrophy

❑ Retinal hemorrhage

❑ Chorioretinal exudates

❑ Lipemia retinalis

❑ Central retinal artery occlusion

❑ Central retinal vein occlusion

❑ Angioid streaks

❑ Hyperviscosity

Clinical Findings

Hypertension  A significant AV crossing change is one that is two disc diameters out and that obliterates the venous column of blood. This is because of longstanding arterial muscular hypertrophy, and it will remain even after the hypertension is treated. Accelerated hypertension is most readily recognized by retinal hemorrhage, which is a marker for a similar pathophysiology in the brain.

Diabetic retinopathy  Diabetic retinopathy most often involves microaneurysms, dot hemorrhages, and exudates. Neovascularization around the optic disc heralds retinal and vitreous hemorrhage, which leads to blindness.

Glaucoma  The optic cup-to-disc ratio is increased, and striations can be seen on the surface of the cup. The cup is several diopters deep, with vessels visibly rising over the lip of the disc.

Cholesterol emboli  A brightly refractile yellow embolus impacts at an arteriolar branch point. This is important to recognize as a marker of an ulcerated carotid plaque.

Papilledema  The optic disc becomes edematous, which is manifest as an indistinct disc margin, hyperemia, and absence of venous pulsations. The usual implication is raised intracranial pressure.

Pigmented crescent  This is a normal finding adjacent to the disc, and its appearance corresponds to the degree of skin pigmentation.

Macular degeneration  Macular drusen, atrophy of the retinal pigment with prominent choroidal vessels, subretinal edema or hemorrhage, and a central fibrous scar are typical findings.

Retinal detachment  The retina appears to billow in undulating folds. It is difficult to keep vessels in focus because they cross focal planes.

Acute optic neuritis  On examination it appears very similar to papilledema, but there is decreased visual acuity as opposed to an enlarged physiologic blind spot.

Optic atrophy  It appears as a porcelain-white disc with sharply demarcated edges.

Retinal hemorrhage  Retinal hemorrhage is found in accelerated hypertension, diabetes, pernicious anemia, DIC, leukemia, and subarachnoid hemorrhage. In endocarditis, a Roth spot (focal hemorrhage with a clear center) may be found.

Chorioretinal exudates  Cytomegalovirus retinitis in a patient with AIDS has an appearance of a yellow granular exudate with hemorrhage at the advancing border. These should be distinguished from the cotton-wool spots caused by HIV infection alone. White cotton-like lesions in a febrile immunocompromised patient suggest systemic candidiasis.

Lipemia retinalis  The retina and retinal vessels have a pale yellow appearance in hypertriglyceridemia.

Central retinal artery occlusion  The optic disc is pale, the retina is edematous, the macula appears cherry-red, and there are “boxcar veins.”

Central retinal vein occlusion  Veins are tortuous and dilated, the retina is edematous and has flame hemorrhages, and the optic disc margin is blurred.

Angioid streaks  Dark linear streaking of the retina in pseudoxanthoma elasticum appears like ghosts of traversing vessels. This condition is associated with accelerated peripheral vascular and coronary artery disease.

Hyperviscosity  Tortuous sausage-link retinal veins are found in
macroglobulinemia.

» READ BOOK EXCERPT ONLINE »

Source: Field Guide to Bedside Diagnosis, 2007

Macular degeneration: Causes
(Handbook of Diseases)

Age-related macular degeneration results from the formation of drusen (clumps of epithelium) or subretinal neovascular membrane in the macular region. It may be hereditary. Cigarette smoking and lack of antioxidants, such as vitamins C and E, may also enhance occurrence.

Underlying pathologic changes occur primarily at the level of the retinal pigment epithelium, Bruch’s membrane, and choriocapillaris in the macular region. Drusen (bumps), which are common in elderly people, appear as yellow deposits beneath the pigment epithelium and may be prominent in the macula.

» READ BOOK EXCERPT ONLINE »

Source: Handbook of Diseases, 2003

Scotoma: Medical causes
(Signs & Symptoms: A 2-in-1 Reference for Nurses)

Chorioretinitis

Chorioretinitis, inflammation of the choroid and retina, produces a paracentral scotoma. Ophthalmoscopic examination reveals clouding and cells in the vitreous, subretinal hemorrhage, and neovascularization. The patient may have photophobia along with blurred vision.

Glaucoma

With glaucoma, prolonged elevation of IOP can cause an arcuate scotoma. Poorly controlled glaucoma can also cause cupping of the optic disk, loss of peripheral vision, and reduced visual acuity. The patient may also see rainbow-colored halos around lights.

Macular degeneration

Macular degeneration results in a central scotoma. Ophthalmoscopic examination reveals changes in the macular area. The patient may notice subtle changes in visual acuity, in color perception, and in the size and shape of objects.

Migraine headache

Transient scintillating scotomas, usually bilateral and typically homonymous, can occur during a classic migraine aura. Besides pain, characteristic associated symptoms include paresthesia of the lips, face, or hands; slight confusion; dizziness; and photophobia.

Optic neuritis

Inflammation, degeneration, or demyelination of the optic nerve produces a central, circular, or centrocecal scotoma. The scotoma may be unilateral with involvement of one nerve, or bilateral with involvement of both nerves. It can vary in size, density, and symmetry. The patient may report severe vision loss or blurring, lasting up to 3 weeks, and pain — especially with eye movement. Common ophthalmoscopic findings include hyperemia of the optic disk, retinal vein distention, blurred disk margins, and filling of the physiologic cup.

Retinitis pigmentosa

Retinitis pigmentosa initially involves loss of peripheral rods; the resulting annular scotoma progresses concentrically until only a central field of vision (tunnel vision) remains. The earliest symptom — impaired night vision — appears during adolescence. Associated signs include narrowing of the retinal blood vessels and pallor of the optic disk. Eventually, with invasion of the macula, blindness may occur.

» READ BOOK EXCERPT ONLINE »

Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007

Scotoma: Medical causes
(Nursing: Interpreting Signs and Symptoms)

Chorioretinitis.Inflammation of the choroid and retina produces a paracentral scotoma. Ophthalmoscopic examination reveals clouding and cells in the vitreous, subretinal hemorrhage, and neovascularization. The patient may have photophobia along with blurred vision.

Macular degeneration.Any degenerative process or disorder affecting the fovea centralis results in a central scotoma. Ophthalmoscopic examination reveals changes in the macular area. The patient may notice subtle changes in visual acuity, in color perception, and in the size and shape of objects.

Optic neuritis.Inflammation, degeneration, or demyelination of the optic nerve produces a central, circular, or centrocecal scotoma. The scotoma may be unilateral with involvement of one nerve, or bilateral with involvement of both nerves. It can vary in size, density, and symmetry. The patient may report severe vision loss or blurring, lasting up to 3 weeks, and pain—especially with eye movement. Common ophthalmoscopic findings include hyperemia of the optic disk, retinal vein distention, blurred disk margins, and filling of the physiologic cup.

Retinal pigmentary degeneration.Retinal pigmentary degeneration causes premature retinal cell changes leading to cell death. One disorder, retinitis pigmentosa, initially involves loss of peripheral rods; the resulting annular scotoma progresses concentrically until only a central field of vision (tunnel vision) remains. The earliest symptom—impaired night vision—appears during adolescence. Associated signs include narrowing of the retinal blood vessels and pallor of the optic disk. Eventually, with invasion of the macula, blindness may occur.

» READ BOOK EXCERPT ONLINE »

Source: Nursing: Interpreting Signs and Symptoms, 2007


 » Next page: Risk Factors for Age-related macular degeneration

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