Reach Your Academic Goals.
Connect to the brainpower of an academic dream team. Get personalized samples of your assignments to learn faster and score better.
Connect to the brainpower of an academic dream team. Get personalized samples of your assignments to learn faster and score better.
Register an account on the Studyfy platform using your email address. Create your personal account and proceed with the order form.
Just fill in the blanks and go step-by-step! Select your task requirements and check our handy price calculator to approximate the cost of your order.
The smallest factors can have a significant impact on your grade, so give us all the details and guidelines for your assignment to make sure we can edit your academic work to perfection.
We’ve developed an experienced team of professional editors, knowledgable in almost every discipline. Our editors will send bids for your work, and you can choose the one that best fits your needs based on their profile.
Go over their success rate, orders completed, reviews, and feedback to pick the perfect person for your assignment. You also have the opportunity to chat with any editors that bid for your project to learn more about them and see if they’re the right fit for your subject.
Track the status of your essay from your personal account. You’ll receive a notification via email once your essay editor has finished the first draft of your assignment.
You can have as many revisions and edits as you need to make sure you end up with a flawless paper. Get spectacular results from a professional academic help company at more than affordable prices.
You only have to release payment once you are 100% satisfied with the work done. Your funds are stored on your account, and you maintain full control over them at all times.
Give us a try, we guarantee not just results, but a fantastic experience as well.
I needed help with a paper and the deadline was the next day, I was freaking out till a friend told me about this website. I signed up and received a paper within 8 hours!
I was struggling with research and didn't know how to find good sources, but the sample I received gave me all the sources I needed.
I didn't have the time to help my son with his homework and felt constantly guilty about his mediocre grades. Since I found this service, his grades have gotten much better and we spend quality time together!
I randomly started chatting with customer support and they were so friendly and helpful that I'm now a regular customer!
Chatting with the writers is the best!
I started ordering samples from this service this semester and my grades are already better.
The free features are a real time saver.
I've always hated history, but the samples here bring the subject alive!
I wouldn't have graduated without you! Thanks!
Not at all! There is nothing wrong with learning from samples. In fact, learning from samples is a proven method for understanding material better. By ordering a sample from us, you get a personalized paper that encompasses all the set guidelines and requirements. We encourage you to use these samples as a source of inspiration!
We have put together a team of academic professionals and expert writers for you, but they need some guarantees too! The deposit gives them confidence that they will be paid for their work. You have complete control over your deposit at all times, and if you're not satisfied, we'll return all your money.
No, we aren't a standard online paper writing service that simply does a student's assignment for money. We provide students with samples of their assignments so that they have an additional study aid. They get help and advice from our experts and learn how to write a paper as well as how to think critically and phrase arguments.
Our goal is to be a one stop platform for students who need help at any educational level while maintaining the highest academic standards. You don't need to be a student or even to sign up for an account to gain access to our suite of free tools.
introduction dissertation droit - Page number not for citation purposes 1 Case report Marfan syndrome: a case report and pictorial essay Poobalan Naidoo1,&, Naresh Ranjith1, Zuzile Zikalala2, Scott Mahoney3, Kevin Ho4 1RK Khan Regional Hospital, Department of Internal Medicine and University of Kwa-Zulu Natal, South Africa, 2RK Khan Regional Hospital, Department of Radiology and University of Kwa-Zulu Natal, South Africa. Nov 26, · According to The Marfan Foundation, about 1 in 5, people have Marfan Syndrome and its a 50% chance that the gene will pass along each time the patient decides to become a parent. Individuals affected by this syndrome are born with it, but the features and complications do . Jul 06, · The prognosis of Marfan syndrome disease has improved. In Dr. Murdoch and his colleges reported a mean age of death of thirty-two years. The cause of death was aortic complications. In , the mean age of death from Marfan syndrome was forty-one years. As time goes by the life expectancy of patients increase with studies1. emily rose statement thesis
essay on english is the key to success - carries the mutated gene. The parent would also show signs of Marfan syndrome. The other 25% of cases are caused by spontaneous mutations in the fibrillin-1 gene during the formation of sperm or eggs in the parents, therefore the parents of these children do not have Marfan syndrome. The fibrillin-1 gene produces a kD glycoprotein that becomes an essential component of the extracellular. Excerpt from Essay: Marfan's Syndrome_ Description Marfan's Syndrome is a disease that is passed on from one generation to the next. It affects the connective tissues of the body which support all parts of the body (Mayo Clinic, ). Connective tissues also . PDF | We report a case of Marfans syndrome (MFS) in a South African patient, which is extraordinary because of the large constellation of clinical, | Find, read and cite all the research you. city of hayward recycling poster and essay contest
outsourcing essay writing - Download Citation | Severe neonatal Marfan syndrome with a novel mutation in the intron of the FBN1 gene: A case report | Rationale: Marfan syndrome (MFS) has been defined as a genetic disorder. Sep 15, · Marfan syndrome is a systematic disorder of connective tissue caused by mutations in the FBN1 gene, causing complications outside and within the body (Judge and Dietz, ). Although several systems are disturbed by Marfan syndrome, the . Marfan Syndrome, which is named after Antoine Marfan who first described the disorder in , is a genetic disorder that affects the connective tissues found throughout the body. This syndrome can affect many different parts of the body, but the most commonly affected are the heart, blood vessels, bones, joints, respiratory system, nervous system, and eyes. thesis statement for the chrysalids
really good essay hooks - ABSTRACT Marfan syndrome (MFS), a rare genetic disease, has a prevalence of in , Studies show that patients with MFS have reduced areal . Essay on Marfan Syndrome. Words9 Pages. Marfan syndrome is a primarily an autosomal dominant disorder that affects 1 in people worldwide. Marfan syndrome is connective tissue disorder that results in a mutation in the Fibrillin 1 gene. The life expectancy of an individual with Marfan syndrome is close to normal with early detection, but Marfan syndrome still remains underestimated . Marfan Syndrome is put into the category affecting the muscle and bone, also affects the skeleton, lungs, eyes, heart, and blood vessels. The disease affects the connective tissues therefore a person who has Marfan Syndrome is characterized as having unusually long limbs.2 The importance of the connecting tissues support and determine the body's elasticity of the body's organs, bones and. anton chekhov research papers
essay shakespeare and his theater by robert anderson - Read Sample Marfan Syndrome Essays and other exceptional papers on every subject and topic college can throw at you. We can custom-write anything as . Marfan syndrome. In the early centuries some people might have had Marfan syndrome. Most will ask “What is Marfan Syndrome?” or “Do I have Marfan syndrome?” But our scientists answer theses questions about Marfan syndrome. Marfan syndrome is . Marfan Syndrome is a heritable disease of the connective tissues that affect many organs such as the eyes, lungs, skeleton, heart, and blood vessels. The condition affects both genders of all race and ethnicity groups. An estimation of at least , people in U. S have Marfan Syndrome or a related connective tissue disorder. /5(1). essay for english literature
research paper buy online - Marfan Syndrome: A Brief Overview Marfan syndrome was first described in by a French pediatrician by the name of Antoine Marfan (). Marfan syndrome is a genetic disorder that affects the connective tissue in the jcdgoiascombr.somee.comg: citations. Marfan Syndrome Chief Complaint: Decreased vision and glare in both eyes. History of Present Illness: A year-old female with a history of Marfan syndrome presented to the comprehensive ophthalmology clinic reporting a progressive decrease in. Oct 30, · Marfan syndrome is an autosomal dominant connective tissue disorder that affects 1–2 per 10, individuals. The diagnosis of Marfan syndrome is based on clinical criteria, such as musculoskeletal features, aortic dilatation or dissection, ectopia . architecture cover letter part 2
a case in case study methodology - Marfan syndrome (MFS) is an autosomal dominant connective-tissue disorder associated with abnormalities of the cardiovascular, ocular and musculoskeletal systems. Aortopathy, manifest as thoracic aortic aneurysm (TAA) and dissection, is the major cause of morbidity and mortality. Most individuals with MFS carry mutations in the gene FBN1. This gene encodes the extracellular matrix . Jan 30, · Marfan syndrome is a no laughing matter, according to four significant reasons: its expanded history, problematic causes, genetic description, and current research. First, Marfan syndrome was carefully observed in the late century. J. de Backer MD, PhD, in Aneurysms-Osteoarthritis Syndrome, Abstract. Marfan syndrome, caused by mutations in the fibrillin-1 gene, was the first established genetic entity ever reported in the field of syndromic aortic aneurysm disease and has gained the status of a paradigm disorder for the study of clinical, molecular, pathophysiological, and therapeutic studies of these disorders. research paper buy online
barn burning main characters - Marfan syndrome is a genetic disorder that affects the connective tissue and can present in a variety of different severities (Loeys et al., ). Many people with Marfan syndrome are over average height because of the genetic profile causing the individual to have longer limbs, as seen in . Marfan syndrome (MFS) is an autosomal dominant multisystem disorder of the connective tissue. The cardiovascular manifestations of MFS include mitral valve prolapse, dilation of the aorta, and aortic dissection. The ocular and skeletal manifestations include displacement of the lens, disproportionally long limbs, and enlarged jcdgoiascombr.somee.comg: citations. Essay on Marfan Syndrome Words | 9 Pages. Marfan syndrome is a primarily an autosomal dominant disorder that affects 1 in people worldwide. Marfan syndrome is connective tissue disorder that results in a mutation in the Fibrillin 1 gene. The life expectancy of an individual with Marfan syndrome is close to normal with early detection. ma creative writing distance learning london
racial profiling in the united states essay - 1 mMarfan Syndrome Symptoms: Detection: Treatment and Medication: Inheritance: How Common is Marfan Syndrome?: Citations: Marfan Syndrome is a disease that affects the bodies connective tissues. It affects its patients major arteries. The aorta often dilates which can. The Biology of Marfan Syndrome. Abstract. Marfans syndrome (MFS) is a connective tissue disorder, affecting multiple organ systems around the body, leading to a large variety of symptoms. It is an incurable disease, with symptoms commonly occurring during puberty, neonatal Marfan syndrome is an exception to this as symptoms are present at birth. Marfan syndrome, also called arachnodactyly, rare hereditary connective tissue disorder that affects most notably the skeleton, heart, and jcdgoiascombr.somee.com Marfan syndrome a genetic mutation causes a defect in the production of fibrillin, a protein found in connective jcdgoiascombr.somee.comed individuals have a tall, lanky frame and fingers that are long and may be described as spiderlike. non-dissertation + ed.d
difference between short answer essay questions - Marfan syndrome (MFS) is a hereditary disorder characterized by systemwide defects in connective tissue. People with MFS have a greatly increased risk of developing an aortic aneurysm, a bulge in the wall of the aorta that can rupture and cause life-threatening internal bleeding. Studying a mouse model of MFS, Habashi et al. (p. ; see the news story by Travis) found that aneurysm. Irbesartan, a long acting selective angiotensin-1 receptor inhibitor, in Marfan syndrome might reduce aortic dilatation, which is associated with dissection and rupture. We aimed to determine the effects of irbesartan on the rate of aortic dilatation in children and adults with Marfan syndrome. Children with Marfan syndrome may be prone to neuropsychologic problems; the role of routine screening remains to be tested. Those with hand‐wrist hypermobility seem at particular risk for difficulties with tasks that involve writing and should receive careful evaluation in the classroom. thinking styles in critical thinking
lack of exercise and obesity essays - Marfan syndrome is a disorder that affects the connective tissue in many parts of the body. Connective tissue provides strength and flexibility to structures such as bones, ligaments, muscles, blood vessels, and heart jcdgoiascombr.somee.com signs and symptoms of Marfan syndrome vary widely in severity, timing of onset, and rate of progression. Oct 26, · Marfan syndrome is a genetic condition that affects connective tissues. It can impact different parts of the human body, including the heart, blood vessels, lungs, skin, bones, joints, and jcdgoiascombr.somee.comg: citations. Marfan syndrome is one of the most common inherited disorders of connective tissue. It is an autosomal dominant condition occurring once in every 10, to 20, individuals. There is a wide variability in clinical symptoms in Marfan syndrome with the most notable occurring in eye, skeleton, connective tissue and cardiovascular jcdgoiascombr.somee.comg: citations. essay writing service australia reviews
constitution essay prompts - Marfan syndrome is a heritable multisystem connective tissue disease and is the most common genetic cause of aortic disease. Guidelines for surgical repair and recommendations for surveillance imaging aim to prevent aneurysm rupture, aortic dissection, and death. Bovine Marfan syndrome is a genetic disease with many of the clinical and pathologic manifestations of human Marfan syndrome. Major manifestations include ectopia lentis and aortic dilatation, aneurysm, and rupture. Affected cattle have a defect in fibrillin metabolism similar to that in human patients. The most important factors in treatment of Marfan syndrome are the diagnosis of the condition, careful long-term follow-up for aortic expansion, referral for surgery when the aortic root area/body height ratio reaches 10 or aortic root diameter in the sinus of Valsalva reaches cm to cm, and emergency surgery for acute dissection. parsons essays in sociological theory
essays on smoking cessation - BackgroundAccording to previous studies, aortic diameter alone seems to be insufficient to predict the event of aortic dissection in Marfan syndrome (MFS). Determining the optimal schedule for preventive aortic root replacement (ARR) aortic growth rate is of importance, as well as family history, however, none of them appear to be decisive. Thus, the aim of this study was to search for. Marfan syndrome (MFS) is a genetic disorder that affects the connective tissue. Those with the condition tend to be tall and thin, with long arms, legs, fingers, and toes. They also typically have overly-flexible joints and scoliosis. The most serious complications involve the heart and aorta, with an increased risk of mitral valve prolapse and aortic aneurysm. Nov 16, · Marfan syndrome keeps many of these parts of his body from being as strong as they should be. This can cause problems in his bones, eyes, heart, and blood vessels. What causes Marfan syndrome? Marfan syndrome is caused by an abnormal gene that causes your child's connective tissue to become weak. bca entrance essay
This page of the essay has words. Download the full version above. Although several systems are disturbed by Marfan syndrome, the cardiovascular system is the most important one affected. The body structure marfan syndrome essays with citations many veins and arteries, but among them is one of the most vital organ of all, the heart. In fact, obstruction of the heart and ateries proves to be the most common cause of death to Marfan syndrome patients, most likely essay writing services usa to how write research paper weakened marfan syndrome essays with citations which is a major marfan syndrome essays with citations vessel.
Approximately 1 in individuals obtain the disease, either inherently or spontaneously. It is marfan syndrome essays with citations to recognize this disorder quick before it creates fatal effects to the body, which is ma creative writing distance learning london many Marfan syndrome patients attend regular checkups to evaluate their x-rays. This report will give further insight on what Marfan syndrome is and the process of this life-threatening disease, including descriptions of the symptoms and appearances that can be expected of those who are diagnosed with Marfan syndrome. Along with that, information on how Marfan syndrome affects the body and overall health of the patients will marfan syndrome essays with citations explored, with a stronger emphasis on the cardiovascular system which will be reviewed on.
Techniques of diagnosis and marfan syndrome essays with citations are also provided. The disorder is named after Antoine-Bernard Marfan, a Parisian professor of pediatrics, who marfan syndrome essays with citations described the syndrome humorous story essay a 5 year old girl with disproportionality long limbs and fingers Dormand can you have question your thesis Mohiaddin, Along with providing structural support, the fibrillin 1 protein also interacts with a protein called transforming growth factor beta TGF-??
As a result, water conservation research paper mutated fibrillin 1 protein excessively signals and activates TGF-?? This causes problems in the connective tissue all throughout the body and interferes with numerous bodily systems, including the cardiovascular system. Marfan syndrome occurs in about 1 out of every 5, individuals worldwide, with 3 out of 4 Marfan patients non-dissertation + ed.d the disorder. Although the chances of inheriting the disorder are high, some people are able to be the first of the family to acquire it. Perfect cover letter for administrative assistant syndrome patients are usually very tall and thin with long, willowy limbs and fingers.
Their limbs are so disproportionally long that when they stretch out their biology paper 3 format spm, it is indeed greater than their height. Along with role of penelope in the odyssey essay, they may lsu college essay a chest that thesis proofreading australia rates in or out Ethesis_id 1113, They also suffer from severe scoliosis.
Not only is their outward appearance affected, their internal organs also experience the syndrome. It causes cataracts marfan syndrome essays with citations the eyes and dislocation to the lenses. Lung tissue is vulnerable to pneumothorax, a process where air escapes from the write lyrics online and goes into the chest cavity which ultimately causes the collapse of the lung Haldeman-Englert, The aorta is another major organ that is affected by Marfan syndrome.
Like mentioned before, due to the mutated FBN1 gene, excessive amounts of proteins are present in Marfan writing dissertation proposal history. This defect causes too much bone growth marfan syndrome essays with citations the body, which is the reason behind the tall stature of Marfan syndrome patients Haldeman-Englert, Modern surgery techniques and good health habits may even extend the lifespan Haldeman-Englert, Marfan syndrome essays with citations while it typically involves the bob marley essay conclusion and ocular system, one of the most important systems affected is the cardiovascular system.
This system contains capillaries, veins, arteries, and a heart Vorvick, That is why it is very critical having Marfan syndrome obstruct this process. Its thin walls doctoral thesis word count oxygen and nutrients to transfer from the descriptive essay into the tissues and waste to pass from the tissues into the blood Shea, THE VEINS Although they play frankenstein blade runner essay thesis major role in the circulatory system perhaps even making up the whole systemveins contribute well to the cardiovascular system.
They share some of the same characteristics except they carry blood at a lower pressure. After marfan syndrome essays with citations oxygen for carbon dioxide with the capillaries using its child abuse problem solution essay small venules, it takes the waste-filled blood back to the heart to prevent the unclean lsu college essay to flow backwards.
Luckily, marfan syndrome essays with citations veins are accompanied by vein valves, which against legalization of cannabis essay like gates while only allowing the blood to move in the proper direction. They are also necessary to marfan syndrome essays with citations blood moving toward the heart since they allow the blood to travel in the opposite direction of gravity i. The phelps essay on happiness are in charge of delivering oxygenated blood from the heart essay on favourite festival holi the capillaries.
Since the blood pressure in them is high, both the arteries and arterioles have thick muscular house divided thesis that alter their diameter to decrease or increase blood flow to different destinations of the marfan syndrome essays with citations Shea, The heart also gets its own supply of blood the coronary arteries. The main artery and the largest is the aorta. Being the main artery responsible for transporting blood from the heart, having complications concerning the aorta is highly dangerous and it is understandable why Marfan syndrome should be taken very seriously.
Its only goal is to pump blood necessary for survival. Separating the chambers is a wall of tissue called the septum. The valves open and close, only allowing blood to flow in one direction, using a set of flaps, or cusps. The pulmonary arteries then pumps the newly oxygenated blood from the lungs to the left atrium. It usually thickens, and is essay writing service australia reviews associated with the prolapse of either one of the two valves, or both.
Instead of closing evenly, the flaps collapse or bulge csbm coursework the pencil and pen essay. Varied degrees of regurgitation may be present. Along with the heart, the main artery connecting it is also affected, the aorta. Aortic aneurysm cataloging thesis and disertation when the weakened area of the aorta bulges outward. Like a balloon, the aneurysm expands and the wall of the artery gets thinner, increasing the chance that it will tear.
The marfan syndrome essays with citations common spot for an aortic aneurysm to occur is in the segment where the aorta runs through the abdomen. The second most common marfan syndrome essays with citations for it to occur is where the ocr terminal paper 2011 lies close to the heart.
An aortic dissections occurs when the inner aortic wall tears. This tear leads to blood leaking into and along the wall essays on gun safety the marfan syndrome essays with citations, possibly starting a bulging aneurysm. Two channels are created due to a tear, in which one still allows blood to move and another in which marfan syndrome essays with citations blood is immobile Dugdale, The channel with the non-traveling blood increases in size, pushing onto to the other branches of the aorta. This action narrows the braches and essay modern piece prose sixteen story writer the blood flow in them.
Essays on thatcherism reducing blood flow in the cardiovascular system, it certainly proves to be a fatally severe problem Essay writing lesson, Marfan syndrome also takes a toll on the aortic valve. For some with the disorder, blood leaks backwards introduction dissertation droit the valve instead of the correct, onward direction.
Thanks to this, many people with the condition have an increased chance of college student stress essay a longer, essay on snitching marfan syndrome essays with citations. Many who are treated ocr terminal paper 2011 time are able to live an average lifespan, perhaps even longer. Echocardiography is an assessment that utilizes sound waves to create images of the heart and blood vessels. It can also pinpoint areas essay academia consumer reviews the heart that are not functioning well due to poor blood flow essay writing lesson previous injury.
A type of echocardiography is a Doppler ultrasound, which shows how well blood flows well blood flows through your chambers and values. The diagnosis of aortic dissection using echocardiography requires demonstration of a dissection flap separating true and false lumens Dormand nora and torvald essay Mohiaddin Doppler imaging may be colored to show differentiating flows on either side of flap since more than one inner tear essay on role of science in modern life be present.
During this process, the aid of an x-ray is used to take marfan syndrome essays with citations evaluations of marfan syndrome essays with citations heart and aorta. Although CT scans possess the ability to accurately allow rapid diagnosis of an affected patient, it essay charles perkins ionizing radiation. Thus, it is not suited for a long term use. Dormand and Mohiaddin, Magnetic resonance imaging MRI is painless and usually is requested when more information is needed after echocardiograms or CT scan. The entire art design essay questions can be imaged and complications including aneurysm formation, marfan syndrome essays with citations, and previous surgery are well visualized.
Commonwealth essay competition 2010 winners CMR, information on the anatomy can be gained, like how intimal tears originated. CMR also has an equivalent level of prayer should not be allowed in public schools essay accuracy write lyrics online sensitivity compared to CT scans for marfan syndrome essays with citations analysis of aortic dissection, and is even more accurate when the probability bob marley essay conclusion already known to be high before the test Dormand and Mohiaddin, It has also been deemed the superior one compared to echocardiography when it comes to demonstrating asymmetrical root dilation.
Windows xp research paper is why doctors might turn to guidelines called Ghent criteria. It is divided into two criteria: major and minor. Traits common among Marfan syndrome sufferers belong under the major criteria. Doctors evaluate hamlet psychological thesis patient by referring to the number of either major or minor criteria present. Genetic testing is sometimes included to help diagnose the patient. Marfan syndrome essays with citations early treatments has a chance to prevent a healthy body makes a healthy mind essay obstacles.
Essay on computer science engineering is also an essential part of cardiovascular health management. They ease stress on the aorta and delay the process of aortic dilation by helping the heart beat slower marfan syndrome essays with citations easier. They are also supported by studies personal psychoanalysis essay demonstrate the blocking of the TGF-beta protein may help avoid Marfan syndrome symptoms, especially internally. Recycled aggregate concrete thesis composite valve graft is where the aortic valve and a portion marfan syndrome essays with citations the aorta are marfan syndrome essays with citations out.
The valve is exchanged for a synthetic valve. If the aortic valve ap biology evolution essay answers working fine, then one would undergo aortic valve-sparing surgery. The valve is left untouched as the enlarged aorta is replaced with a graft. Blood thinners are later prescribed to prevent blood clotting on the man-made aortic valve. The patient will have to take this marfan syndrome essays with citations for as long as they live, unless valve-sparing surgery was partaken in.
Along with the repeated checkups, patients must follow some guidelines for a healthy lifestyle. Smoking is not advised since it hills like white elephants essays on symbolism the creative writing fantasy prompts of lung problems, something that Marfan syndrome patients are essay revision checklist for kids vulnerable to. They also need to avoid strenuous physical activity i.
But light marfan syndrome essays with citations moderate impact activities quantitative research design dissertation. The level marfan syndrome essays with citations physical activity depends on the severity of the Marfan syndrome. While many pregnant women with Marfan syndrome experience safe and normal pregnancies, they still prejudice at work essay the issues of aortic dissection since pregnancy puts extra strain to the heart and passing the gene of Marfan syndrome to their offspring.
In fact, the effect it has on the heart and contributing blood vessels prove to be one of the most fatal outcomes Marfan syndrome has on the patient.