Cushing’s Syndrome Cushing’s Syndrome is a condition that results from chronic exposure to excessive amounts of glucocorticoids circulating in the blood stream for an extended period of time. The disease was first reported by Harvey Cushing over one hundred years ago‚ yet the condition still plagues endocrinologists today. Reasons for this difficulty include the vast amount of often vague symptoms that the syndrome presents‚ most of which are found in a plethora of other conditions as well‚ combined
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Charge Syndrome Introduction Charge Syndrome is a specific collection of non-randomly occurring congenital anomalies. The acronym CHARGE actually stands for the major features of this syndrome. The letter C stands for coloboma of the eye‚ H is heart defects‚ A stands for atresia of the choanae‚ R is retarded growth and development‚ G stands for genital abnormalities and lastly letter E stands for ear anomalies and/deafness. The cause of this syndrome may be genetically heterogeneous‚ but
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Asperger’s Syndrome In today’s society‚ Asperger’s Syndrome is being talked about‚ and seen‚ more than ever‚ from television shows‚ such as Parenthood‚ to magazine articles‚ and of course in the inclusive classroom. Throughout this paper we will be looking at where Asperger’s Syndrome originated‚ some of the characteristics and causes‚ as well as ways in which teachers and parents can better deal with a child that has Asperger’s Syndrome. Asperger’s Syndrome is found under Autistic Spectrum
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Mental Illness Research Questions - Munchausen Syndrome What illness are you researching? Factitious Disorders Munchausen Syndrome Ganser Syndrome What is the definition of your disorder? What might be physical/noticeable characteristics of this disorder? Munchausen syndrome is a mental disorder where a person repeatedly pretends to have severe illnesses‚ when they actually are the ones causing the illness to themselves. Those who have this illness will mostly complain of physical pain‚ as opposed
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Turner Syndrome It was first described in 1930‚ and first diagnose in 1959. Now a days‚ 1 of 2‚000 females are born with this syndrome. Turner syndrome (also known as TS) is named after the famous endocrinologist Henry Turner‚ who was the first person to described and published any findings about this syndrome. This condition is also known as Bonnevie-Ullrich syndrome‚ Gonadal dysgenesis‚ and Monosomy X. The syndrome is a non-inherited chromosomal condition that only occurs in females. It’s cause
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Introduction This paper will explore the case study of Suzanne‚ an independent living 25-year-old woman with Downs Syndrome that presents with progressively worsening congenital heart and lung abnormalities. She has been referred to a transplant center to be evaluated for a possible heart-lung transplant. The transplant center will be in charge of determining whether or not she will be able to handle her post-transplant care. In order to make this determination‚ “A Guide to Moral Decision Making”
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flenfef Down Syndrome is named after John Langdon Down‚ the first British doctor who first described the condition in 1987. It wasn’t until 1959‚ however‚ that an extra chromosome was identified as the cause. One in every 691 babies in the the United States are born with Down syndrome. Making Down syndrome the most common genetic condition. Approximately 400‚000 Americans have Down syndrome and about 6‚000 babies with Down syndrome are born in the United States each year. Down syndrome (DS)‚ also
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Down Syndrome Thesis: When someone sees a child or an adult with Down syndrome they automatically single them out‚ every person in this world is different‚ with a disability or with out‚ but that doesn’t mean they need to be treated differently. I. Causes A. Mental Disorder B. Mothers age C. Not inherited D. Most common E. Amniocentesis II. Symptoms A. Problems at birth B. Size C. Other issues D. Facial features III. Severities A. Ranges B. Trisomy 21 C. Mosaic D. Mosaic
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DOWN SYNDROME Down Syndrome is a congenital disorder arising from a chromosome It comes from a defect involving chromosome 21. The condition leads to impairments in both cognitive ability and physical growth that range from mild to moderate developmental disabilities. Through a series of screenings and tests‚ Down syndrome can be detected before and after a baby is born. The only factor known to affect the probability of having a baby with Down syndrome is maternal age. Less than one in 1‚000
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Williams syndrome also recognized as Williams-Beuren syndrome is a genetic disorder caused by a deletion of more than twenty five genes from chromosome 7. Although Williams syndrome is often non-hereditary‚ the chances of the syndrome being passed on if an individual with Williams syndrome has a child are fifty percent. Individuals born with Williams syndrome often possess distinctive facial features which make the syndrome easily recognized. These features include wide spaces between their teeth
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