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    Angelman Syndrome

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    Angelman syndrome is a rare genetic disorder that affects around 1 in around 12,000-20,000 live births and affects both males and females equally. Angelman syndrome is very often misdiagnosed as autism or cerebral palsy. Angelman syndrome is not an inherited disease, and is instead caused by a change in the E3 ubiquitin protein ligase gene (UBE3A) on the maternal chromosome 15. This change prevents the chromosome from functioning properly. It occurs as a random event during the formation of eggs…

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    Recognized as Safe) (1). Research on probiotics has shown efficacy of probiotic bacteria on a variety of health problems. GI difficulties such as antibiotic-associated and acute infectious diarrhea, Inflammatory Bowel Disease, and Irritable Bowel Syndrome have demonstrated responsiveness to probiotics. In addition, probiotics also have shown activity in influencing the host’s immune system (1). With growing research on probiotics and the integral role they play in health, and with…

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    Williams Syndrome Essay

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    Overview: What is Williams Syndrome? Definition: Williams Syndrome is a genetic disorder, resulting from the deletion of 26 or more genes one chromosome number 7 (Mervis et al., 2000). That seemingly small loss can affect numerous parts of a person’s physical and mental health, as well as social behavior and sensory perception (Genetics Home Reference, 2014). Diagnosis: Williams Syndrome is a genetic condition that a child is born with and it can impact a child’s prenatal development as well…

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    Harry Angelman Syndrome

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    In 1965 Harry Angelman reported clinical findings in three children with similar, unusual, attributes. These children had what was known as “happy puppet” syndrome, but was later changed to Angelman syndrome, due to its pejorative name. Angelman syndrome is a neurodevelopmental disorder distinguished by: severe learning difficulties, ataxia, jerky movements, epilepsy, speech impairments, hypopigmentation in the hair and the skin with blue eyes, subtle dysmorphic facial features, and happy and…

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    Adrienne Bashista Speech

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    The speaker Adrienne Bashista gave a very insightful speech about what Fetal Alcohol Syndrome is and how it is caused. Before our speaker told us about her son, I had very little knowledge about what FASD was. I now realize how severe FASD is and how even the slightest consumption of alcohol can affect a fetus during pregnancy. I became aware that FASD is a rare syndrome that only 2 to 5 percent of the population have. This statistic surprised me due to a large amount of woman who may drink when…

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    Williams Syndrome (WS) is a rare genetic disorder that affects approximately 20,000 people in the United States. This condition is present at birth. The causes of Williams syndrome is due to the deletion of 26 plus genes on one of an individual’s chromosome #7. Individuals born with Williams syndrome share a number of common neurological, medical, and behavioral characteristics as well as common facial…

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    If a child is suspected to have a developmental delay they will be evaluated. These skills are age related and will vary by age. The evaluations will take place in such areas as gross motor skills, which encompasses the usage of large muscle groups for movement. These movements include walking, running, and sitting. Gross motor skills are also important for balance. Fine motor skills are motor movements that use smaller more refined muscle movement. These would be using pincer skills needed to…

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    Angelman Syndrome Description of the Disease An extremely rare and uncommon disease known as Angelman Syndrome is a very complex neurodevelopmental and monogenic disorder (Bailus, 2014). The term neurodevelopmental refers to the shape, reshape, state and generation of the nervous system during the embryonic stages of life, while the term monogenic can be explained as a disease, which is controlled and inherited, by a single pair of genes (Gentile, 2009). It is estimated that Angelman Syndrome…

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    Fragile X Research Paper

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    Fragile X is a syndrome that I had little to no knowledge about before the presentation that Denise Devine gave us. From the presentation, I learned an array of information that will be helpful in my future. Denise touched upon a few topics that are important when understanding Fragile X syndrome. Fragile X the most common forms of mental impairment and is an inherited syndrome that is one of the leading developmental disabilities. One significant fact that is surprising is that Fragile X became…

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    Dr Keith Case Summary

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    appreciate. The complete tender point exam was performed and he is positive in 12 of the 18 classic tender points. He also has some induration over the right trapezius tender point that is more classic for the trigger points of a myofascial pain syndrome than the tender point of fibromyalgia. Other interesting historical…

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