01/29/2003. The SSA granted disability benefits because of borderline intellectual functioning and pervasive developmental disorder. She had a history of Apert’s syndrome
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the disease. Progeria Research Foundation also funds medical research that is specifically aimed at finding the cause. Treatments and cures for this syndrome are more reasons that the foundation funds research for the disease (How PRF was formed). Progeria is an outcome of a fault in the Lamin A(LMNA) gene (Hutchinson-Gilford Progeria Syndrome 2012). The LMNA gene has codes that are for two proteins‚ Lamin A and Lamin C. These proteins play a big role in stabilizing the inner membrane of
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Prevention for Noonan Syndrome looks slightly different than other disorders‚ due to the fact that it is genetically linked. With cases of NS being linked to different genetics and some cases having an unknown origin‚ it is hard to prevent the disorder from occurring. A big factor towards prevention lies in the education of the people closest to the patient‚ the community‚ and the general public. A very effective preventive way would be to administer genetic testing to the population in order to
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Rett Syndrome for Girls Only Rett syndrome is very rare neurological disorder that affects the brain. The disorder primarily effects girls only‚ but there has been reported cases of males with the disorder. The disorder is rare‚ it effects one in every 10‚000 to 15‚000 females‚ in all racial and ethnic groups. Rett syndrome effect one in every 100‚000 males. Rett Syndrome impairs the child’s speech‚ motor functions‚ daily activities‚ and respiratory functions. Rett Syndrome is usually diagnosed
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Rett Syndrome Abstract 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
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s Rett’s Syndrome Website: http://understandingrettsyndrome.webs.com History Rett Syndrome is a developmental disorder experienced almost always in girls‚ and is first recognized during infancy. Before the discovery of this disorder‚ incidents of Rett Syndrome were mistaken for many other neurologic disorders such as Autism‚ Cerebral Palsy‚ or Nonspecific Developmental Delay‚ especially in females. An Austrian physician‚ Dr. Andreas Rett‚ first described this
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Down Syndrome Down syndrome is a genetic condition that typically causes some level of learning disability and a characteristic range of physical features. Most babies born with Down’s syndrome are diagnosed with the condition after birth and are likely to have: reduced muscle tone leading to floppine eyes that slant upwards and outwards a below average weight and length at birth Although children with Down’s syndrome share some common physical characteristics‚ they do not all look the same
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Münchausen Syndrome and Münchausen Syndrome By Proxy Münchausen Syndrome There are many syndromes in people’s lives. All of the sydromes have been effecting people’s health negatively in people lives since the existence of human being. One of the most interesting syndrome is Munchausen Syndrome. It is related to unreal illness. In other words‚ Some people who has münchausen syndrome can cause an illness own their own. Therefore‚ they are actually clever and have medical information. Due to their
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Down Syndrome (DS) is the most common chromosomal condition in the United States‚ affecting about 1 in every 700 babies (CDC). This condition is also known as Trisomy 21‚ due to there being an extra copy of chromosome 21 (CDC). This extra chromosome results in changes in the development of the brain and body‚ which in turn can lead to cognitive and physical challenges (CDC). Some hallmark physical characteristics include almond shaped eyes that slant up‚ smaller hands and feet‚ shorter stature‚
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Korsakoff’s Syndrome Korsakoff’s syndrome is a disorder in which a lack of thiamine results in anterograde and retrograde amnesia — those with the disorder exhibit the loss of newly formed memories‚ and a degeneration in their ability to remember events from their past (Spiegel‚ Lim‚ 2011‚ p. 15). Found generally in alcoholics‚ the combination of their compromised metabolism and thiamine deficiency results in Wernicke’s Encephalopathy‚ which then progresses to Korsakoff’s syndrome (Thompson‚ Guerrini
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