Sundowning Syndrome Etiology and Treatment 12/3/2010 Anatomy & Physiology sundowning syndrome: etiology and treatment An escalation in disruptive behaviors in the late afternoon and early evening among institutionalized patients suffering from dementia and Alzheimer’s disease has been a recognized phenomenon for over 60 years (Bachman & Rabins‚ 2006). The timing of the onset of disruptive behaviors has led to calling this phenomenon sundowning‚ sundowning syndrome‚ and nocturnal delirium
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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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She did not eat and did not care about her personal hygiene when drinking alcohol. The Comparison Point Decision (CPD) date was 01/29/2003. The SSA granted disability benefits because of borderline intellectual functioning and pervasive developmental disorder. She had a history of Apert’s syndrome
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Noonan Syndrome Noonan syndrome is a genetic disorder that was once known as Turner-like syndrome. It is a mutation of several genes where they develop proteins that are continuously active; which ends up disrupting the control of the cells growth and division resulting in abnormal developments of the body. Noonan syndrome can affect a person’s physical appearance in multiple ways‚ along with their mental state of mind. This syndrome equally affects males and females. Noonan syndrome was first
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Reducing the number of pregnancies and sexually transmitted infections (STIs) among those aged under 16 is a government priority due to rising numbers of both (Department of Health‚ 1999; 2001; Social Exclusion Unit‚ 1999). Contraceptive nurses have a key role as they are in a unique position to give clients the opportunity to talk about intimate areas of their sexual life and anxieties in a non-judgemental environment (Everett‚ 1998). Most agencies offering information‚ advice or services on sexual
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Rett Syndrome Abstract Rett syndrome is considered one of the autism spectrum disorders. Rett syndrome is a developmental disability disorder resulting in severe mental and physical deficits in female children. Rett syndrome is grouped as a pervasive developmental disorder (PDD) in which conditions are severe and pervasive‚ and that begin in early life and influence multiple areas of development. Rett syndrome‚ including the age of onset and the severity of symptoms‚ varies from child to
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CheckPoint: Pre-Socratic Philosophers * Answer the following questions in a 200- to 300-word response: * Which of the Pre-Socratic philosophers had the most compelling ideas? I believe that for their time‚ all held compelling ideas as to how things are in existence; the pre-Socratic philosophers that “stuck out” most to me were The Atomist. By far‚ The Atomist was the closets philosophers to what we the human race holds as true. * Briefly summarize the philosopher’s idea
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Victoria Haskins Biology Honors Mr. Kelly March 6th‚ 2017 Edwards Syndrome Edwards syndrome‚ also known as Trisomy 18‚ is a condition caused by a mistake in meiotic cell division resulting in an extra chromosome 18 in a developing baby (Source 1). This condition disrupts normal development‚ potentially fatally‚ even before birth (Source 1). Major characteristics of the disorder include a delay in growth‚ a low birth weight‚ and other major medical complications (Source 1‚ Source 3). Professor of
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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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22q11.2 deletion syndrome‚ several tests have to be conducted in order to determine if this is in fact the cause. With our proband‚ it is clear that this is a case of familiar inheritance. As a clinician‚ is it important to start by asking about the patient’s current and past medical history‚ history of present illness‚ developmental and social functioning and obstetric history so we can get a more in depth understanding of the patient’s presentation (“22q11.2 Deletion Syndrome”‚ 2016). A physical
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