normal 44-year-old‚ 6 ft. [183 cm] tall man of average intelligence. [edit] Effects [edit] Physical traits XYY syndrome typically causes no unusual physical features or medical problems. Males with this syndrome may be slightly taller than average and are typically a few centimeters taller than their father and siblings. Skeletal malformations may also accompany XYY syndrome at a higher rate than in the general population. Severe facial acne has occasionally been reported‚ but dermatologists
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Dumping Syndrome My Digestive System Disorder essay is about the Dumping Syndrome. Dumping Syndrome occurs after meals in people who had gastric bypass surgery. The Dumping Syndrome has two type of forms the early dumping syndrome and late dumping syndrome. Dumping Syndrome causes dizziness sweating and weakness. To help decrease the symptoms of the dumping syndrome involves changes in diet and nutrition. Dumping Syndrome is mostly found in African Americans that eat mostly sugar and its moves
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Intrinsic and extrinsic means inside and outside. Examples of intrinsic factors Biological structures like peel to inhibit microorganisms‚ pH‚ moisture content‚ RedOx potential‚ nutrient content‚ antimicrobial constituents‚ presence of other microorganisms‚ Examples of extrinsic factors Low pH‚ low temperature‚ addition of nitrites‚ casing and packaging to inhibit microbial growth. : http://www.leadership-central.com/types-of-motivation.html#ixzz4XrtSpRVa . Teratogens: Any mediator that can disturb
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A symptom of ASD is when you struggle with social interaction and communication. Some children with ASD don’t babble or use any other vocal sounds‚ language development tends to be delayed in children with ASD‚ they may also lack awareness and interest in other children. They tend to play alone or gravitate towards a differently aged group instead of playing with others their age. They may find it hard to understand other emotions and feelings‚ and can have difficulties starting and/or taking part
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Blue Rubber Syndrome is a rare condition initially discovered by Gascoyen in 1860. In 1985 William Bennett Bean made the disease more popular for which the disease was termed Bean Syndrome. Later referenced Blue Rubber Bleb Nevus Syndrome‚ this disease causes patients blood vessels to develop improperly in an area of the skin or visceral organs‚ particularly the gastrointestinal (GI) tract. The malformed blood vessels form blood clots and appear on the skin as deep blue‚ soft‚ and rubbery blebs
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White syndrome is a heart defect in which the heart has an extra electrical pathway that causes a rapid heartbeat. Wolff- Parkinson- White syndrome is usually found in patients who has family members that has been diagnosed with this disease. Approximately one third of all Wolff- Parkinson- White syndrome patients will develop auricular fibrillation. Auricular fibrillation is a cardiac arrhythmia that is seen in patients with pathway problems in the heart. Wolff- Parkinson- White syndrome can be
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Psychologists are brought in as expert witnesses in court on many occasions including battered woman syndrome and automatism syndrome. In both syndrome’s people have a strong opinion one-way or the other with little ability to believe in a middle ground when deciding if they believe in the syndrome or if they do not. Battered Woman Syndrome (BWS) - "The syndrome denotes a set of distinct psychological and behavioral symptoms that result from prolonged exposure to situation of intimate partner
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The History of Fragile X Syndrome. The first appearance the Fragile X syndrome was in 1943 when doctors Martin and Bell discovered that a specific form of mental retardation was X-linked. Both go on to describe a pedigree of X-linked mental disability. (Martin & Bell‚ 1943). Fragile X Syndrome has not been around for that long‚ actually less than eighty years. Later in 1969‚ Herbert Lubs a doctor developed the chromosomal test for Fragile X chromosome. Lubs accomplished this chromosomal test by
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Project Waardenburg Syndrome Brian Tokay March 4‚ 2011 Waardenburg Syndrome is an inherited disorder characterized by different levels of hearing loss and changes in hair and skin pigmentation. A common trait of Waardenburg Syndrome is different colored eyes or very bright blue eyes‚ a low hairline‚ connected eyebrows‚ some may have a patch of white hair or grey hair by the age of twelve‚ and a wide space between the eyes. There are at least four types of Waardenburg Syndrome-Types 1‚2‚3‚and
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suffers from the disease known as Morquio Syndrome‚ which affects his metabolism. The disease presents when the body is missing or doesn’t have enough of a substance needed to break down long chains of sugar molecules called glycosaminoglycans. Morquio Syndrome is a rare inherited birth defect that is estimated to occur in one of every 200‚000 birth. The disease may not be visible at birth but symptoms usually begin between ages 1 and 3. Morquio syndrome is an inherited condition‚ which means it
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