Retinitis Pigmentosa Essay

but not all ROP complications can be treated do you sacrifice sight for brain function?

The dry form is broken down into three stages; Early, Intermediate, and Advanced (National Eye Institute 3). In the Early stage, people have several small or few medium yellow deposits under the retina called drusen. This stage shows no symptoms or vision loss. During the second stage, Intermediate, more medium or even large deposits happen. As this happens, a blurred spot can develop and more light could be needed for reading. Lastly, in the Advanced stage, a breakdown of light-sensitive cells and tissue causes the blurred spot to enlarge and darken. In this latter stage, facial recognition is unlikely unless the person is extremely close. Either form of Macular Degeneration can only be detected by thorough eye exams. The exam should include visual acuity, which measures sight at varied distance intervals. Also, dilation of the eyes will allow an ophthalmologist to check the retina and optic nerve. An instrument called a Tonometer will measure pressure within the eyes (National Eye Institute 6).

As discussed in Dr. Fink’s lecture, high blood pressure can result in retinal damage. This retinal damage can present as hemorrhages, exudates, or with a component of papilledema (CP, 145). According to Lilly, this retinal damage produced by hypertension is termed hypertensive retinopathy. More often than not, the retinopathy can be seen on physical exam but is asymptomatic to the patient. However, the clinical presentation can help to further classify the nature of the patient’s hypertension.

Retinitis pigmentosa is a group of inheritable diseases that is characterized by gradual deterioration of the photoreceptors in the retina. The photoreceptor cells in the retina, rod cells, are light sensitive cells that are able to sense low levels of light. The frequency of retinitis pigmentosa is one in four thousand births (Deng et al., 2015; Fahim et al., 2012; Haddad et al., 2016; Shu et al., 2012) People affected by retinitis pigmentosa will typically exhibit symptoms of night-blindness first, and this will precede a loss in the patient’s visual acuity field that starts from the outer edge and gradually moves inward resulting in a much smaller visual field and loss of peripheral vision, also known as tunnel vision (Haddad et al., 2016).

To understand the diverse causes of RP, a basic understanding of visual perception is required. Phototransduction (conversion of light to electrical signals) occurs first, which is initiated by two types of photoreceptors: rods and cones. These two types vary in their function as rods are primarily responsible for night vision and lack sensitivity to color while cones function in color vision. Light contacts these photoreceptors, and isomerizes a retinaldehydechromophore (retinal) which is bound to varying types of opsin proteins corresponding in their reactivity to different wavelengths of light. Upon absorption of a photon of light, the chromophore 11-cis-retinal is isomerized to the all-trans confirmation, which subsequently causes a series of molecular interactions which ultimately result in the electrical response of the photoreceptors (Vugler 2010). As 11-cis-retinal is required to absorb photons of light, this compound must be regenerated, a function that is performed with the aid of nearby cells of the retinal pigment epithelium

Rett syndrome is considered one of the autism spectrum disorders. Rett syndrome is a developmental disability disorder resulting in severe mental and physical deficits in female children. Rett syndrome is grouped as a pervasive developmental disorder (PDD) in which conditions are severe and pervasive, and that begin in early life and influence multiple areas of development. Rett syndrome, including the age of onset and the severity of symptoms, varies from child to child. Before the symptoms begin, however, the child generally appears to grow and develop normally, although there are often subtle abnormalities even in early infancy, such as loss of muscle tone (hypotonia), difficulty feeding, and jerkiness in

For the health condition description of age-related macular degeneration I will discuss the etiology, onset, prevalence rate, body systems, body structures, and associated deficits that come and are associated with this disease. “AMD is the degradation of the cells at the center of the retina which is the layer of tissue at the back of the eye that registers light. The macula is responsible for ventral vision, which enables us to read, drive, participate in sports, and do anything else that requires focusing directly ahead. Macular degeneration distorts the heart of the vision field” (Macular degeneration, 1998). Sunlight and smoking are both influences of the onset of AMD (Age-related Macular Degeneration (AMD), 2014). It is suggested to avoid intense bright sunlight which may help reduce the retinal degeneration. Hats, sunglasses and any other accessories that can help protect the eyes from the sun are suggested. Cigarette smoking has also been linked to increasing the risk of developing AMD and it is recommended that persons should stop smoking to decrease their chance of developing AMD (Age-related Macular Degeneration (AMD), 2014). AMD does not develop until the sixth or seventh decade of life, although early

Retinal vein occlusion is the second leading cause of vascular disorder after diabetic retinopathy.1 Retinal vein occlusions are classified into 3 categories depending on the location of the thrombus formation; branch retinal vein occlusion (BRVO), central retinal vein occlusion (CRVO), and hemi retinal vein occlusion (Hemi-RVO). 7 BRVO is considered to be the most common among the retinal vein occlusions.6 BRVO occurs more often in men than women. Asians (5.7 per 1000) and Hispanics (6.9 per 1000) are at greater risk of developing BRVO than other ethnicities.6 The age range of patients diagnosed with retinal vein occlusion ranges from young as 14 years of age to old as 92 years of age, with 51% of patients being older than 65 years.3 Advancing age is an important risk factor for developing retinal vein occlusions. Prevalence of retinal vein occlusions in 40-49 years old is 1.57 per 1,000, 4.58 per 1,000 in 50-59 years old, 11.11 per 1,000 in 60-69 years old, 12.76 per 1,000 in 70-79 years old, and 10.32 per 1,000 in those older than 80 years.6

As humans, we don't always see with our eyes, but often with our imagination (Grunwald, 2016). Often times as people we never realize how useful our vision really is to us. You really don't think about something like that until it would actual happen to you. Throughout this essay, you will learn how the body is affected by Macular Degeneration (MD). Different signs and symptoms, as well as the etiology of MD, will be discussed. In the following, diagnosis tests and treatments may also be listed in order to help others who would like to know more about MD. Not to mention, you will learn the incidence and progression of MD. Furthermore, information though agencies and associations, as well as new research about MD will be given.

Patients with age-related macular degeneration may not notice any symptoms at first. The first noticeable sign is a gradual, or sudden, change in the quality of vision depending on which type of AMD is occurring. Straight lines will start to appear distorted (Kozarsky, 2017). Early dry AMD is diagnosed by the presence of drusen. This gradually can cause a dramatic loss of the center of vision. In the intermediate stage of AMD, the beginnings of vision loss are apparent, but there still may not be any other noticeable symptoms. At this time, optometrists will test for larger drusen and pigment changes in the retina (“Research into the Genetics of Macular Degeneration,” 2017). Other symptoms of age-related macular degeneration might include an

For each patient, the automated visual field tests were obtained by Humphrey Field Analyzer and optic disc images by Topcon fundus camera. Horizontal and vertical cup-to-disc ratios were calculated by a manual, planimetric technique. Mean deviation (MD) and pattern standard deviations (PSD) were documented.

Retinitis pigmentosa(RP) is an inherited, degenerative eye disease that causes severe vision impairment due to the progressive degeneration of the rod photoreceptor cells in the retina . Retinitis pigmentosa is one of the most common inherited diseases of the retina, affecting 1.5 million people worldwide. Up to 150 mutations are known to cause retinitis pigmentosa, which includes three genetic inheritance patterns- autosomal dominant inheritance, autosomal recessive inheritance, or X-linked inheritance. Symptoms often first appear in childhood that patients would endure nyctalopia, the decreasing vision at night or in low light, then lost of peripheral vision causing “tunnel vision” and finally,

Retinitis Pigmentosa 3 is blindness caused by the progressive death of rod and cone photoreceptors in the retina. This is a genetic disease, that can be inherited in autosomal dominant, recessive

     Macular Degeneration is a problem in the part of the eye that controls your sharpest central vision. It is a group of diseases that result in a loss of detailed vision. The brain will not just leave the spot empty, so it learns to fill it in with spotty macular cell damage. People most of the time don't tell their doctors (opthalmologists) about it until it is well in advance.

Cornea-Independent is correct visual impairment without affecting the cornea, which organized into non-surgical Interventions and surgical