Genetic disorder Essays

  • Jonathan Jackson's Genetic Disorder

    1400 Words  | 6 Pages

    decision to strip Jonathan Jackson of his job because of his genetic disorder, Haemophilia. They believe that Jonathan Jackson will be unable to function in his role as an air traffic controller. It will also investigate whether their employers should be given the right to make decisions based on their medical information from their DNA and then make this information available to other future employers. Haemophilia is a rare bleeding disorder in which the blood doesn 't clot normally. If someone has

  • Genetic Disorders Booklet: Polydactyly Case Study Answers

    1142 Words  | 5 Pages

    Genetic disorders booklet: polydactyly Q. Who first discovered the genetic disorder? How was it discovered? A. Tyler Steven Hayden was the one who discovered the disorder. Q. is the disease state dominant or recessive? Explain. A. polydactyly is a dominant but rare disease, it’s caused by a dominant allele of a gene. It can also be passed down if one of the parents have the disorder. Q. Differentiate between recessive and dominant disorder? Explain. A. your genes

  • Genetic Disorders: Cystic Fibrosis

    652 Words  | 3 Pages

    Cystic Fibrosis is a serious genetic disorder that affects the insides of a human body. Cystic Fibrosis is a genetic condition in which the lungs and the insides of the human body become clogged with thick sticky mucus. The mucus builds up inside of the body and affects the insides like the lungs, liver , pancreas, your sinuses, and more. Cystic Fibrosis also affects the digestive system which makes food harder and a longer time to digest. Some symptoms for cystic fibrosis are salty-tasting skin(sweat)

  • Genetic Disorders: Color Blindness

    594 Words  | 3 Pages

    The genetic disorder I chose to study is color blindness. Being Color blind is actually very common for men and not as much for women. Color Blindness affects one in twelve men and one in two-hundred women. Color Blindness is also known as color vision deficiency or CVD, and is stated in the article, "Color Blindness" by Utah Eye Centers, that it is "an abnormal condition characterized by the inability to clearly distinguish different colors of the spectrum." That just basically means that some colors

  • Genetic Disorders: Sickle Cell Anemia

    572 Words  | 3 Pages

    Sickle cell anemia is a genetic disorder it is also known as sickle cell disease. A genetic disorder is something that is passed down from parent to child. This is a disease of the hemoglobin. Hemoglobin is a red protein responsible for transporting oxygen in the blood of vertebrates. Sickle cell anemia causes your red blood cells to stiffen, although your red blood cell are supposed to be flexible. They need to be flexible because they have to fit through small and large spaces. The red cell turns

  • Zellweger Syndrome Research Paper

    1017 Words  | 5 Pages

    Zellweger syndrome is an autosomal and recessive disease. It is part of one a 4 disease of disorders known as peroxisomal biogenesis disorders. It is caused by absence of peroxisomes, which remove the body of toxic substances in the liver, brain, and kidneys. The most common features the zellweger syndrome patients include swell liver, high levels of copper and iron in the blood, and vision disturbances. This disorder results from the inheritance by 2 mutations genes for one of the receptors (PXR1) needed

  • Prader Willi Syndrome Research Paper

    1115 Words  | 5 Pages

    general population” (Butler n.p.). Prader Willi Syndrome was discovered in 1956 after Andrea Prader, Alexis Labhart, and Heinrich Willi noticed nine children with the same characteristics of PWS. Prader Willi Syndrome is a genetic disorder that is incurable

  • Duchenne Muscular Dystrophy Research Paper

    927 Words  | 4 Pages

    Dystrophy Introduction Duchenne Muscular Dystrophy is a dangerous and rare disorder. It is transferred through family generations because it is a genetic disease. Duchenne Muscular Dystrophy is referred to by many names including DMD, Duchenne Syndrome, and Pseudohypertrophy. DMD is when the body cannot make dystrophin so it results in muscle weakness. Mode of Inheritance Duchenne Muscular Dystrophy is a X-linked recessive disorder and that is why DMD is more common in males. Women can only be a carrier

  • Jurassic Park: Movie Analysis

    1094 Words  | 5 Pages

    The movie Jurassic Park became an international sensation when it was released in 1993. It changed the cinematic art of storytelling. It was widely recognized as a high watermark in computer graphics (Timeline, 2015). The reason for these accolades was the extensive computer-generated imagery (CGI) that was used throughout the movie. Before Jurassic Park, CGI was used but not to this extreme that director Steven Spielberg demanded. • 1985: Young Sherlock Holmes - Stain Glass Man, first completely

  • Huntington's Disease Research Paper

    1448 Words  | 6 Pages

    What is the autosomal dominant neurodegenerative disease Huntington’s Disease? How does this disease affect the patient throughout their lifespan? In 1872 George Huntington, a young medical doctor discovered Huntington’s Disease as an inherited disorder. He published a paper On Chorea, better known today as Huntington’s Chorea. Huntington’s Chorea is defined as involuntary erratic muscle contractions. Dr. Huntington’s research helped pave the way for future doctors. In 1993 a group of scientists

  • The Benefits Of Genetic Testing

    1022 Words  | 5 Pages

    Genetic testing is the process of examining DNA where the DNA is examine for chromosome, genes and proteins changes. Mainly used to detect genetically inherited disease, if the individual is a carrier of a genetically inherited disease or any possible presence of genetically inherited disease, but this method can also be used to determine a child's biological parents, a person's ancestry (usually to make a family tree), finding genetic diseases in the fetus, screening embryos for diseases, and figuring

  • Research Paper On Huntington's Disease

    1050 Words  | 5 Pages

    Huntington’s Disease Introduction Genetic diseases are caused by any abnormality that might occur in an individual’s genome. Some genetic disorders are transmitted or inherited from parents to their offspring while others are caused by acquired mutation or changes in an already existing gene. Mutations can take place randomly or due to some environmental factors. There are different modes of genetic disorders that include single gene and multifactorial inheritance, chromosome abnormalities, and

  • Ethical Issues In Genetic Counselling

    1519 Words  | 7 Pages

    Genetic Counselling, Ethical Issues in Management of Hemoglobinopathies 1. Describe the risk assessment in genetic counselling. (how to diagnose the disease) (why is it important to have a genetics counsellor) Genetic counselling is a way of communication between a doctor and patient and this may include parents/family. The importance of having a genetic counselor is so that the counselor receiving the genetic tests and family history is there to help advice patients (and parents/family) about the

  • Risks In Genetic Counselling

    1169 Words  | 5 Pages

    Determining the recurrence risks in genetic counselling is very important. Risk of being affected by a particular genetic disorder is based on the genetic nature of the disorder and the pedigree of the particular family being counselled. The family member being counselled is usually a relative of the proband. Risks for single gene disorders can be estimated by using basic Mendelian principles, while the risk calculation might be complicated in disorders with decreased penetrance, variability of expression

  • Marfan Syndrome

    640 Words  | 3 Pages

    Marfan syndrome is not the only genetic disorder that affects connective tissue and has conditions including Thoracic Aortic Aneurysm. Marfan syndrome is a genetic disorder that messes with the connective tissue throughout the body (Marfan Foundation) and was discovered by Antoine Marfan in France back in 1896 (KidsHealth). Features of this genetic disorder are mostly found in the heart, blood vessels, bones, joints, and eyes. (Marfan Foundation) But it affects each person differently. Marfan can

  • Human Genetic Modification

    1245 Words  | 5 Pages

    Human genetic modification is the manipulation of genes in human DNA so that defective genes don’t obstruct proper functioning, and so that inherited diseases are not passed on. Those against it may argue that genetic modification is simply unnecessary, immoral, or interferes with nature’s course. However, genetic modification overall is and will continue to be beneficial to the mental and physical health of the entire human species. Falling under the umbrella of biology, it is sensible to consider

  • Aarskog Syndrome Research Paper

    479 Words  | 2 Pages

    Aarskog Syndrome Description Aarskog syndrome (also known as Aarskog–Scott syndrome, faciodigitogenital syndrome, shawl scrotum syndrome and faciogenital dysplasia) is a rare autosomal X-linked inherited disorder that affects a person 's height, muscles, skeleton, genitals, and appearance of the face. It mostly affects at birth and the symptoms usually become apparent by the age of 3years. Unfortunately, Aarskog syndrome is a lifelong condition without a cure. Some people with Aarskog syndrome

  • The Pros And Cons Of Genetic Screening

    822 Words  | 4 Pages

    we should understand how genetic screening works and consider both the benefits and risks of this matter. Ethical, social, and medical factors all play a role in determining this. Genetic screening is where DNA samples are used to identify gene or genes related to a genetic disease or disorder. It determines risk of having or passing on a genetic disorder and detects some genes known to cause genetic disorders. Preimplantation genetic diagnosis is a specific type of genetic testing done in-vitro process

  • Cognitive Therapy Research Paper

    1974 Words  | 8 Pages

    Cause As stated before depression is on a complex spectrum of mood disorders. There is no single definition so describe depression. There is no one form of it either, the fluidity of this mood disorder covers a wide area of disorders. Just like depression is a multidimensional disorder it also multidimensional when it comes to causation. However it is understood to be caused by a combination of genetic, biologic, environmental and psychological factors (Health, 2011). Genes are one of the basic

  • What Are The Pros And Cons Of Gene Therapy

    1196 Words  | 5 Pages

    existing cells to prevent and possibly cure various diseases. The new gene can alter the way the cells behave by destroying the mutated version to modify its effects or by replacing a faulty gene. The main target of treatment in gene therapy are genetic disorders (Better Health, 2017). Gene therapy is still in its experimental phase and scientists are not yet sure of not only what all it can do, but what long-term effects treated patients may