Abnormality Essay

Overview Noonan syndrome is a disorder caused by a genetic mutation that causes various parts of the patient’s body to develop abnormally. The condition occurs when a parent passes on an affected gene to their child that produces constantly active proteins, leading to a disruption in the process of normal cell division and growth. Science currently knows of eight genes in which a mutation can cause the disorder. In some cases, there is no family history and the mutation is spontaneous. Symptoms

I write with an update on Ms. Walker, whom I saw at Bentley Memory clinic as an outpatient for a follow up review. Clinical issues: 1. Subjective reports of memory problems: Recent PET scan did not support the diagnosis of Alzheimer’s disease 2. Bipolar affective disorder: currently in remission 3. Medical co-morbidities: hypertension and GORD History and Assessment: As you are aware, Ms. Walker is a 65-year-old retired welfare officer, living in a Homes west unit independently, who is known with

(Meriggioli and Sanders, 2012). Abnormalities of the thymus can lead to the development of the autoantibodies that target AChR, which ultimately triggers muscle weakness (Meriggioli and Sanders, 2012). . One pathological path of MG starts with antibodies against AChR, and this is the most prevalent type of MG. AChR myasthenia gravis occurs in 80% of patients that have this ocular or generalized disease, and the autoantibodies that disrupt AChR functions can arise from abnormalities in the thymus (Nacu, Anderson

changes in patient’s condition and to detect for signs of deterioration (Dougherty and Lister 2008 cited in Phillip et al 2013). >>>>>vital signs definition and normal parameters??<<<<<< Up to 80% of adverse events are predicted by physiological abnormalities that occur over hours and sometimes days (Kause et al 2004 cited in pantazopoulos 2012). Early detection of patient deterioration allows for early treatment of infections or hospital acquired pneumonia (Mato 2009, Mato 2010 and Straub 2014). It

Genetic engineering has constantly been a major point of focus in the world of science over several years. From 1989 to present day, many people have questioned not only the process, but the motives behind genetic engineering. Over the years, the term “designer baby” has made the transition from movie screens to dictionaries, where it is defined as “a baby whose genetic makeup has been artificially selected by genetic engineering combined with in vitro fertilization to ensure the presence or absence

begin a quest to map and understand all the genes of human beings. A mere 13 years later and just shy of $3 billion invested the Human Genome Project successfully mapped the billions of base pairs involved. With the ability to diagnose specific abnormalities, researchers and medical professionals have saved hundreds of ill children to which their survival was indefinite. However, with scientists continuing

PGD is a reproductive option for those who do not want to pass on specific genetic disorders or chromosome imbalance to their offspring. After undergoing IVF, embryologist’s will screen the embryos DNA. Embryo’s which contain obvious genetic abnormalities will be excluded and unaffected embryo’s will be transferred to the uterus; therefore, the patient can

If you haven’t heard of the Zika virus by now, you will be hearing about it soon because of the attention it has recently gained. The Zika virus is an infection that is similar to the West Nile virus and yellow fever. The virus was discovered in Uganda in 1947, and is common in African and Asian countries. It only recently was discovered to have spread to Brazil and the Western Hemisphere in 2015. Zika was a rare tropical disease with mild symptoms when it was discovered. It takes its name from

You are a physician and a patient presents with the following symptoms: Stella is a previously healthy 47 year-old woman. She has been experiencing chest pain and a persistent cough. She thinks that she saw a bit of blood during the last coughing fit. She has tried Tylenol cold and flu and drinking cold water, because she suspected she had a cold. She smokes ¾ of a pack of cigarettes a day. She says that she is trying to quit; cutting down from 1 pack/day to ½ pack but recently went back up to ¾

What is Turner Syndrome? Turner Syndrome was named after Dr. Henry Turner who discovered it in 1938, but also referred to as Ullrich-Turner, Bonnevie-Ullrich-Turner, and Gonadal Dysgenesis. This syndrome occurs in 1 out of 200,000 females. Making it a rare syndrome that only 70,000 people in the whole world has. Turner syndrome is a lifelong condition. Most people live long and healthy lives, yet some are susceptible to numerous chronic conditions. Genes are passed on to a child from each parent