Jacquelyn Rivera Biology 1st block March 10‚ 2017 Angelman Syndrome Angelman syndrome is a rare genetic disease because of paternal DNA patterns‚ missing chromosomes‚ and gene mutation. It is caused by many symptoms and there are many signs to know if you have Angelman syndrome. There is treatment for AS‚ but there is no cure. Angelman syndrome (AS) is a neurodevelopment disorder can be caused by genetics. AS causes cognitive disability‚ motor dysfunction‚ speech impairment‚ hyperactive‚ short
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Angelman syndrome is a genetic disorder that cause developmental delay and neurological problems. There is sometimes sleep disturbances‚ seizures‚ jerky movements‚ frequent laughter or smiling and usually always happy. The people that have this tend to not use many words‚ or none at all. Most likely they are very hyper and have little balance. An older term that people use to use would be‚ happy puppet syndrome‚ but it is no longer an accepted term. When people have Angelman syndrome‚ they appear
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multiple traumatic brain injuries caused chronic headaches‚ vision problems‚ and body fatigue. The symptoms of post-concussive syndrome also began to have a significant impact on my education. Activities such as reading‚ completing homework assignments‚ and keeping my attention in class became increasingly difficult. The most unexpectedly traumatic aspect of living with this syndrome was that I could no longer play sports and the teammates I considered to be my friends became more distant. During the
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In this case‚ the patient developed locked in syndrome due the basilar artery thrombosis leading to complete absence of voluntary movement with cognitive function intact. Locked-in syndrome caused basilar artery thrombosis most commonly related to trauma‚ vascular‚ or cardiac malformation‚ as the basilar remain a major supply of posterior circulation; patient with basilar artery thrombosis commonly presented with sudden and dramatic neurological impairment mostly sudden vertigo‚ dysarthria‚ headache
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Klinefelter’s Syndrome “Harry Fitch Klinefelter specialized in endocrinology and rheumatology (weak bones) and through his studies Klinefelter’s syndrome was described in 1942‚” (Encyclopedia Britannica). The diagnosis of the patient is usually done at a young age through a series of many tests‚ one in which the doctor finds if the patient has two X-Chromosomes and one Y-Chromosome. As a random genetic mishap during the formation of the fetus‚ Klinefelter’s has many symptoms. The treatment is not
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phantom limb syndrome is a medical condition in which an amputee is able to perceive sensations from a body part that is long attached to the body. According to McCormick‚ Chang-Chien‚ Marshall‚ Huang‚ & Harden (2013)‚ approximately 80% of amputees experience sensations or pain at some point after an amputation. Sensations during phantom limb syndrome can be described in various ways‚ pain‚ sharp muscle spasms‚ burning‚ stabbing‚ aching‚ pressure‚ and gnawing. The nature of phantom limb syndrome can acute
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Turner syndrome is named after Henry Turner who‚ in 1938‚ was one of the first doctors to report on the disorder in medical literature. Turner syndrome is one of the most common chromosomal disorders and is one of the most common genetic disorders found in females‚ it is a rare chromosomal disorder that affects only females. This condition occurs in about 1 in 2‚500 female births worldwide‚ but is much more common among pregnancies that do not survive to term‚ like miscarriages and stillbirths.
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Post Tubal Ligation Syndrome Are there truly side effects caused by tubal ligation? Candy Layne COM/220‚ Research Writing Instructor Amy McKenzie July 15‚ 2009 Post Tubal Ligation Syndrome Are there truly side effects caused by a tubal ligation? Ever heard of side effects from a simple surgery? How about the procedure causing harsh menstrual cycles? Thousands of women across the U.S. have had this surgery and have the same complaint. The surgery is a tubal
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Genetically transmitted disease Down syndrome Down syndrome is a genetically transmitted disease‚ the symptoms of this disease can vary depending on the person‚ but children with Down syndrome have unique physical characteristic traits for example: decrease in muscular tone‚ excess skin around the nape‚ widened nose‚ among others. Some mental characteristics are: impulsive behavior‚ short periods of attention and slow learning. Some of the disease’s effects are: pulmonary hypertension
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capability of adolescent and adult participants with Williams Syndrome to obtain conceptual change concepts with an empirical approach. These 10 participants with William Syndrome were compared to a few groups of normal developing children with respect to biological knowledge about people‚ animals and plants. The experiment’s final results ended in an engrossing sum of information that effected in the participants with Williams Syndrome being differentially impaired on conceptual change for construction
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