Septo-Optic Dysplasia Research Paper

Eye Vision Inc, a long-standing medical device manufacturer, has signed a contract to sell Holland Hospital the Clear View Laser and a two-year separately priced maintenance plan for $1 million and $0.2 million respectively. On a when-and-if available bais, Eye Vision Inc. will provide software updats that is embedded with the Laser to maintainance purchasor. The software has never been sold without Laser for its functional necessity. In this memo, as explained below, we conclude that:

Duane’s Syndrome is a rare genetic disorder. A Genetic disorder is usually a irregularity in the genes or in the chromosome, these irregularities can be anything from not fully developed, not being there at all, or even having an extra unneeded set. These When someone thinks of a genetic disorder they may think of the very well known disorder of Down's Syndrome, but what people may not know about is the rare disorder called Duane’s syndrome. This syndrome is eye movement limitation syndrome that is usually involved with restricting the eye(s) from moving to the left or right. Moving the eye towards the nose could result in the eye restricting, and/or the eye shooting up or down (Duane syndrome). The simple reason that it is a lesser known

B. Treatments: There is no cure for this disorder, but it can be managed. Being able to live a “normal as possible life” is one of the main focus of treatment (Somatoform Disorders). They will in all probability still have some pain and symptoms. There is one good thing; about this disorder it will not shorten your life. Your physician may prescribe medicine for your symptoms, but in most cases it is not needed. Making your regularly scheduled appointments will help maintain your health.

This disease can cause problems with one's vision, muscle control, balance, and other essential body functions. Up until the age twenty-eight,

A medical definition of vision impairment is a sine qua non that prohibits 20/20 vision in one or both eyes (Bowman, Bowman, Dutton & Royal National Institute for the Blind, 2001; Vision Australia, 2015; Webster & Roe, 1998). Examples of vision impairment include, cataracts, which has the lens inside the eye increasingly cloudy; albinism, which is passed down genetically affecting clear vision and causes sensitivity to bright light; optic nerve damage, which affects field of vision as those nerves controlling vision are disrupted; macular degeneration, where parts of the retina that control colour and fine details are affected; retinitis pigmentosa, which is an ongoing reduction of the field of vision available and nystagmus, where the eye flickers involuntary (Bowman, Bowman, Dutton & Royal National Institute for the Blind, 2001; American Foundation for the Blind, 2015; Vision Australia, 2015 ; Baton Rouge Regional Eye Bank, 2015). John suffers from retinitis

DiGeorge syndrome is a genetic problem due to a defect in the chromosome 22 causing the body systems to be developed poorly. It can result

People with M.S. may have many symptoms. Impaired vision is one in which the optic nerve becomes

is a disease that causes optic nerve damage resulting in the gradual loss of sight. Currently, it is estimated more than 3 million

DiGeorge Syndrome is also known as Velo-Cardio-Facial Syndrome and can affect many parts of the body. This occurs when small pieces of chromosome 22 is missing, resulting in the loss of many important genes. Generally, children with DiGeorge Syndrome have decreased levels of calcium in their bodies, resulting in seizures. These children also typically have underdeveloped, cystic or missing kidneys, compromising the body’s ability to filter waste materials in the blood to make urine. To add, partial immunodeficiency is a common trait of people with DiGeorge Syndrome. This means that these people’s immune systems are not as strong as they should be, making it harder for them to fight infections and disease, resulting in increased illness rates and difficult recoveries from illnesses. As this syndrome affects many parts of the body, heart defects, low platelet counts, difficulty with speech and language, learning difficulties and behavioural disorders are also fairly common in children with DiGeorge disorder. Overall, DiGeorge syndrome has many diverse effects on the human body and is detrimental to the overall wellbeing of those who must live with it.

Moreover, focal cortical dysplasia is a malformation of cortical development. Focal cortical dysplasia is a common cause of intractable epilepsy in children and is a frequent cause of epilepsy in adults. However, FCD includes a spectrum of disordered white and gray matter entities that range from mild cortical disruption to complete derangement of cortical lamination. Patients usually in childhood with refractory partial epilepsy, and subsequent magnetic resonance imaging (MRI) have reveals the area of disordered cortex. Treatment is centered on relieving the seizures and often involves surgical removal of the affected cortex. The defect is thought to arise from a migrational or apoptotic defect occurring early in development. In humans, the

possible diagnosis of ASD. This may be largely connected to the fact that although there is a 60%

The first disease I’m going to mention is Glaucoma, according to Web MD last updated in 2015, Glaucoma is a condition that causes damage to your eye's optic nerve and gets worse over time. It's often associated with a buildup of pressure inside the eye. Glaucoma tends to be inherited and may not show up until later in life.

This condition is often overlooked and treatment delayed because there are no visible signs or abnormalities and children are seldom aware that anything is wrong with their vision.

Sclerosteosis (SCL) is a severe, progressive, autosomal-recessive craniotubular hyperostosis (MIM 269500). The determining gene has been identified as SOST. Sclerosteosis is a sever disorder placing significant hardship on all those who suffer from it. The disorder is characterized by increased bone density. The SOST gene codes for Sclerostin, and a mutation in the gene produces Sclerosteosis. This disorder results in bone overgrowth through life, leading to distortions in facial structure, and entrapment of the 7th cranial nerve. Because of the distortion in facial bones, the cranial nerves can become entrapped, increasing the risk for potentially lethal elevation of intracranial pressure. Recognizing the symptoms is the primary means of diagnosing and treating the disorder.

Caudal nasal septum deviations, despite not being the most common type, cause much complaint, both obstructive as well as cosmetic to the nasal tip. Besides the important functional problems, caudal septum deviations also cause clear cosmetic defects. These change the relation between the columella and the nostrils, causing significant defects on nasal tip position and symmetry (Garcia et al.,