Down Syndrome Learning Disability- a childhood disorder characterized by a difficulty with certain skills. Difficulty in such skills as reading or writing in individuals with normal intelligence. Learning disabilities affect the ability to interpret what one sees and hears or the ability to link information from different areas of the brain. These limitations can show up in multiple different ways. These disabilities extend to schoolwork and can delay learning to read or write. Birth Defect-
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Middle-range theory‚ developed by Robert K. Merton‚ is an approach to sociological theorizing aimed at integrating theory and empirical research. It is currently the de facto dominant approach to sociological theory construction‚[1] especially in the United States. Middle-range theory starts with an empirical phenomenon (as opposed to a broad abstract entity like the social system) and abstracts from it to create general statements that can be verified by data.[2] This approach stands in contrast
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Case Discussion Beal’s syndrome (OMIM # 121050) is a disorder of connective tissues. The syndrome was first explained by Beal’s and Hecht in 1971. It is inherited as an autosomal dominant disorder that is characterized by multiple flexion contractures‚ arachnodactyly‚ severe kyphoscoliosis‚ abnormal pinnae and muscular hypoplasia. It is caused by a genetic mutation in FBN2 gene (encoding the extracellular matrix micro fibril fibrillin 2) on chromosome 5q23. The FBN2 gene provides instructions for
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Tourette Syndrome is a neurological disorder that is characterized by sudden repetitive and involuntary movements or vocalizations that are generally termed “tics”. These tics can have different degrees of intensity ranging from simple to complex. Simple motor tics are brief‚ sudden‚ and repetitive movements that involve a limited number of muscle groups. They include facial grimacing‚ eye blinking and other eye movements‚ and head or shoulder jerking. Simple vocalizations include repetitive sniffing
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member suffer from memory problems? If so‚ it could mean that you have a more serious health condition‚ such as dementia. While dementia can often go unnoticed‚ the caregivers at Visiting Angels in Forty Fort‚ PA‚ the area’s locally-owned leader in home senior care‚ say it’s essential to seek treatment right away to prevent the disease from progressing. To help you better understand dementia and whether or not you or a loved one could be experiencing it‚ take a look at these top five common signs and
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Metabolic syndrome Insulin resistance syndrome; Syndrome X Last reviewed: June 2‚ 2012. Metabolic syndrome is a name for a group of risk factors that occur together and increase the risk for coronary artery disease‚ stroke‚ and type 2 diabetes. Causes‚ incidence‚ and risk factors Metabolic syndrome is becoming more and more common in the United States. Researchers are not sure whether the syndrome is due to one single cause‚ but all of the risks for the syndrome are related to obesity. The
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Progeria Jessica Perry Canterbury School of Florida Progeria is an extremely rare genetic disease which causes young children to age very rapidly. This condition is from the Greek word for old age “geras.” It is estimated that it only affects one in four million newborns throughout the world. A newborn typically will appear normal. Within the year the child’s growth rate decreases and they look shorter and weigh much less than other children around their age. The
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suffering from dementia. This is where the loss of thinking‚ memory‚ and reasoning skills are taking place‚ and a person is significantly impaired to carry out their daily tasks. Symptoms include the inability to remember information‚ asking the same questions over and over again‚ becoming lost or confused in familiar places‚ being unable to follow directions‚ or neglecting personal safety‚ hygiene‚ or nutrition (National Institute on Aging‚ 2009). Some types of dementia include; vascular dementia which is
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Jacob’s syndrome 2 Anatomy and Physiology: Jacob’s syndrome Over the past 40 years people have been aware of Jacobs’s syndrome‚ a rare chromosomal genetic syndrome which occurs when a male receives an extra Y chromosome‚ resulting in a sequence in XYY. Males normally have XY and females normally have XX sequencing 1. Chromosomes store genetic information in all human beings. There are 23 pairs of chromosomes and 46 in total. On the 23rd pair holds the sex chromosomes which also store genetic information
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Noonan Syndrome Nicole Mitchell Dr. Hendricks Principles of Biology 1114 April 19‚ 2013 Mostly everyone in the world has heard of some type of genetic disorder. But most people haven’t even heard or understand about Noonan Syndrome. Noonan syndrome is a genetic disorder characterized by distinctive facial features‚ developmental delay‚ learning difficulties‚ short stature‚ congenital heart disease‚ renal anomalies‚ and bleeding difficulties. Noonan syndrome affects a good percent of the world
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