Polycystic ovary syndrome (PCOS) is a heterogenous condition which disturbs endocrine, metabolic and reproductive function, affecting 6-10% of women of reproductive age. Such a disorder can be defined using the Rotterdam criteria of 2003, which states PCOS is present when two of the following three phenotypes is shown: polycystic ovaries, hyperandrogenism and ovulatory dysfunction. However in recent years, PCOS has been found to present several metabolic consequences such as insulin resistance (affecting
description of your project that starts by stating your clinical question and succinctly explaining your planned intervention in order to orient everyone. The title for this writer’s project is, Polycystic Ovary Syndrome: Lifestyle Modification to Improve Body Mass Index in Obese Women with Polycystic Ovary Syndrome Ages 18 to 44, with a clinical question of, does family based lifestyle modification compared to individual lifestyle modification have a greater impact on BMI in women with PCOS? For the purpose
First discovered in 1935 by Stein and Leventhal, polycystic ovarian syndrome (PCOS) is a complex endocrine and metabolic disorder that is characterized by menstrual irregularity, subfertility and infertility, clinically obvious hyperadrogenism, and metabolic dysfunction in women (Azziz, 2015). Although the etiology of this complex condition is unclear, the prevalence is about 20-40% in women who have mothers and sisters with PCOS, strongly suggesting a genetic association (Azziz, 2015). B.L. presented
Definition: Cushing Syndrome: occurs when your body has been exposed to the hormone cortisol for a long period of time. The most common cause of Cushing’s Syndrome is called hypercortisolism is the use of oral corticosteroid medication. The condition can also occur when your body makes too much cortisol. Cushing’s Syndrome is an endocrine disorder of the adrenal glands, it causes physical and physiological effects. Because of to much cortisol it could cause some hallmark signs: like hypertension
Patient’s safety is essential during hospitalisation and it is everyone concern. It is because, hospital is a place where patients’ injuries are treated, not generated. However, unintentionally injuries may be happen while in the care in the ward. The challenge for nurses are to ensure safety while giving nursing care to them. Falls are the common accidents occurred in ward. This lead harm to patient and emotional stress to the family as well. Throughout my clinical posting, there was an incident
Angel is an 18yo, primigravida, who is currently 29 weeks 4 days as dated by LMP consistent with a 17 week ultrasound performed in an emergency room in North Carolina. She did not have any PNC until 28 weeks due to her move from North Carolina to Tennessee and difficulty with insurance. She has a history of drug use involving benzodiazepines and THC. Once she found out that she was pregnant, which was early on, she stopped using anything. She has had no drug use, per her report, since early first
Polycystic kidney disease is a genetic or hereditary disorder in which clusters of cysts develop within your kidneys. Cysts are round sacs containing water-like fluid. Over time, these cysts will enlarge, multiply and damage the kidneys which can lead to kidney failure. Kidneys are usually the most severely affected organs from this disease, but cysts can also develop in your liver, pancreas, spleen, ovaries, and large bowel. Polycystic kidney disease can also affect the brain and heart. PKD is the
substances needed by the body are reabsorbed back in to the blood stream for future use. There are various pathologies that affect the urinary system due to malfunctioning anatomical structures. In the case of Polycystic Kidney Disease (PKD), the pathology is genetic (Colbert, Ankney & Lee (2013). Polycystic Kidney
Brad Cohen has Tourette syndrome since he was six. Tourette syndrome is known as neurological disorder where people made strange noise, twitches and uncontrollable movements ("Tourette Syndrome Association of Australia is a registered charity to support families and individuals understand and manage Tourette Syndrome.", 2016). Since he was young, his father constantly felt annoyed by this tics and his involuntary movements. He did not really acknowledge Brad for who he was. His mother, on the other
A Rare Disorder called Angelman Syndrome This research paper will discuss a specific disability called Angelman Syndrome. (AS) This Syndrome is a disorder, and can be diagnosed at an early age. AS don’t have a cure, but there are ways to treat this disorder. While reading this paper, you will become aware of the causes, characteristics, diagnoses, assessments and academics of Angelman Syndrome. By the end of the paper you will be able to understand how this disorder affects children and educators
The rare condition Prader Willi Syndrome affects 1 in 10,000 to 30,000 people worldwide. Although this is considered a rare condition it 's actually one of the main reasons there are so many obese people today. “PWS affects males and females in equal numbers and occurs in all ethnic groups and geographic regions in the world. Most estimates place the incidence between 1 in 10,000-30,000 individuals in the general population” (Butler n.p.). Prader Willi Syndrome was discovered in 1956 after Andrea
much sense to me until later on. The whole appointment lasted almost two hours, but it was a very educational two hours, because in the end I found out that I not only had Scoliosis, but that I also had Ehlers Danlos Syndrome (EDS). There are three main types of Ehlers Danlos Syndrome, and I have the hypermobility type. It’s essentially a problem in your body that doesn’t allow you to produce collagen correctly. Unfortunately that affects the way my
Jonathan, a seven and a half year old boy is a social second grader who has normal intelligence. However, Jonathan was diagnosed with spastic cerebral palsy and has dysarthric speech patterns. With spastic cerebral palsy, Jonathan has difficulty regarding his motor control and movement. Confined to his wheelchair, Jonathan works independently, separate from his classmates. Jonathan cannot produce clear speech, his dysarthric speech pattern prevents him from speaking freely in the classroom and
It not so much only the fact that within the story people cannot communicate with each other because of the different language they speak, but it becomes clear how much effect prejudices have on people. Juan Pellicer calls this “a Babelian syndrome: broken communication, misunderstandings, isolation both on the global level as well as in the intimate realm of relations between children and parents, particularly with the consequences of separation and deafness” (Pellicer 240). People are so used to
The expression "pervasive formative issue," likewise called Pdds, alludes to a gathering of conditions that include postpones in the advancement of numerous fundamental abilities. PDD incorporate a few that are described via impeded equal social communication, unusual dialect advancement and limited behavioral collection. There are five sorts of pervasive improvement issue: • autistic issue • asperger's confusion • rett's confusion • childhood disintegrative issue (additionally called disintegrative
In a layman’s term, advocacy is the move to make the voice of the marginalised and vulnerable people heard. Everybody have rights and needs that must be met but some group of people, due to their inability or difficulty to voice out their minds, are unable to meet these needs or demand for their rights and entitlements; when it comes to making decisions that pertain to their lives, their voice and feelings are (sometimes) being ignored and they are treated as if they do not exist. Advocacy is the
Introduction The term kyphosis describes the spinal curve that results in an abnormally rounded back. Kyphosis can happen at any age. 7459 papers were found when the word ‘kyphosis’ was searched on ‘PubMed’ search engine. The majority of these papers studied kyphosis were related with scoliosis. It was understood that kyphosis was studied in addition to the other deformities in the papers related to the etiology of kyphosis with some exceptional cases. Definition Kyphosis is a forward rounding
Autism spectrum disorder and autism are both are both terms for a group of complex disorder of brain development. Autism appears to have to have its roots in very early brain development. However the most obvious signs of autism and symptoms of autism, usually develop between two and three years of age. Both children and adults with autism often show difficulties in verbal and nonverbal Communication, Social interactions, instruction or play. Autism is not something to laugh about. In other words
Developmental prosopagnosia (DP) is a condition in which people have a difficult time recognizing and identifying faces of all people including those they are familiar with. Research surrounding prosopagnosia aims to find differences in reaction time, familiarity and recognition compared to control participants. Shah, Guale, Gaigg, Bird and Cook were looking into the particular mechanisms that cause deficits within the population of people who suffer from developmental prosopagnosia. Specifically
Bioinformatics Project Hutchinson Gilford progeria Syndrome Robert Kelleghan C15386361 DT204/2 Review of the disorder: Hutchinson Gilford progeria syndrome is a rare genetic disorder associated with the accelerated aging in children. The children appear to be normal at birth, however, they begin to face difficulties within their first year of life as they grow slower than other children and fail to thrive (Hui et al, 2011). The affected individuals face many problems