Annotated Bibliography Article Reference Taylor‚ L. and Oliver‚ C. (2008). The behavioural phenotype of Smith-Magenis syndrome: Evidence for a gene-environment interaction. Journal of Intellectual Disability Research‚ 52‚ 830-841. (DOI: 10.1111/j.1365-2788.2008.01066.x) Objective/Purpose Smith-Magenis syndrome (SMS) is not only evident through physical characteristics such as‚ a prominent forehead‚ up-slanting eyes and short stature; but also by developmental delays and moderate to severe
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Down Syndrome Although many theories have been developed‚ it is not known what actually causes Down syndrome. Some professionals believe that hormonal abnormalities‚ X-rays‚ viral infections‚ immunologic problems‚ or genetic predisposition may be the cause of the improper cell division resulting in Down syndrome. It has been known for some time that the risk of having a child with Down syndrome increases with advancing age of the mother; i.e.‚ the older the mother‚ the greater the possibility
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STEVENS-JOHNSON SYNDROME: PATHOPHYSIOLOGY‚ ETIOLOGY‚ DIAGNOSIS AND MANAGEMENT. Roberto Carmona Florida International University Abstract: Steven Johnson Syndrome is an inmune disease charactherized by a detachment of the epidermis from dermis. It could be fatal and the pathophysilogy involves a complex hypersensitivity reaction with the participation of T lymphocytes that induce keratinocyte’s apoptosis. The syndrome can be cause by drigs‚ infections and malignancies. The diagnosis
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KLINEFELTER SYNDROME RESEARCH 1 Klinefelter Syndrome Research Duyen Le Ap Biology KLINEFELTER SYNDROME RESEARCH 2 Abstract Klinefelter syndrome is the most common genetic disorder that affects males. The affected male has an extra copy of X chromosome‚ which means he has 47 chromosomes (XXY). The effects of Klinefelter syndrome vary by age; the patients with Klinefelter syndrome usually have weak muscles‚ slow
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PharmaPoint: Dry Eye Syndrome - Global Drug Forecast and Market Analysis to 2022 th On 8 July 2014 The Dry Eye Syndrome (DES) pipeline is strong‚ with 49 molecules in various phases of development. More notably‚ the late-stage pipeline has three products with novel mechanisms of action to treat the inflammation associated with the disease. That said‚ physicians suggest that the largest unmet need for DES treatment is diagnosis. Browse Full Report @ http://www.jsbmarketresearch.com/he
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Marfan syndrome is a genetic disorder that affects the body’s connective tissue. Connective tissue connects all the organs‚ tissue and body cells together. It also plays an important role in helping the body grow and develop properly. People are born with Marfan Syndrome but they may not notice it until their teen years. The signs and the symptoms of the Marfan syndrome varies. They are so different‚ that people can have the same disease bt they can different symptoms. And with that being said‚ they
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What is is: Posterior Tibial Neuralgia‚ more commonly known as Tarsal Tunnel Syndrome is a painful condition caused by the entrapment or compression of the posterior tibial nerve. Anatomy: The posterior tibial nerve is a branch of the sciatic nerve and innervates the posterior compartment of the legs. As it continues down the leg‚ it passes posteriorly and inferiorly to the medial malleolus. It ends and branches off into sensory branches that innervate the sole of the foot. The tibial nerve travels
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Abstract Munchausen syndrome by proxy is one of the most difficult and rare form of child abuse. It carries substantial morbidity and mortality and comprises both physical abuse and medical neglect and is also a form of psychological maltreatment. The diagnosis relies on appropriate suspicion and careful investigation. Early recognition and appropriate intervention prevent further abuse and criminal actions. The fabrication of a pediatric illness is a form of child abuse and not merely a mental
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Down Syndrome Down Syndrome is a chromosomal disorder. It occurs in about 1 of every 800 births. People with Down syndrome may have mild to severe learning disabilities. Physical symptoms include a small skull‚ extra folds of skin under the eyes‚ and a protruding tongue. People with Down syndrome are subject to a variety of medical problems including heart abnormalities and thyroid gland dysfunction. Survival rates have been increased dramatically in recent years as problems specific to Down syndrome
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Chromosomal Disorder: (Turner Syndrome) Introduction Turner Syndrome is a condition that only alters the development of girls and women. Most girls and women have two full and complete X chromosomes while girls with turner syndrome have only part of the second X chromosome. Women and girls are diagnosed with turner syndrome have features such as slow growth rates‚ a webbed neck‚ broad shoulders‚ and widely spaced nipples. They also have swelling hands and feet‚ heart defects‚ kidney problems‚ and
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