Preview

Edd Genetic Conditions

Good Essays
Open Document
Open Document
555 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Edd Genetic Conditions
Genetic conditions are one or more problems, difficulties, or abnormalities in the genome. Most are present from birth and are very rare. This means they only affect one person in approximately every several thousand or million. These conditions are mainly formed due to mutations in a person’s gene. Genetic conditions have helped scientists a lot due to the different types of genetic conditions there are out in today’s world.

Ectodermal Dysplasia a genetic condition that is not a single disorder. It is built upon several other closely related dysfunctions. ED affects the growth or development of the teeth, hair, nails, and sweat glands. Ectodermal Dysplasia is usually caused by mutations in the EDA gene which are inherited in an x-linked recessive pattern. Some symptoms are absence or malformation of some or all teeth, not being able to perspire which can cause overheating, irregular skin pigmentation, etc. In my opinion i believe ED must’ve been amusing to research and figure out due to all the different abnormalities in one genetic condition, but I’m sure it wasn’t easy either.
…show more content…
This genetic condition is extremely rare because it only happens to 0.01% of all people. Situs Inversus can happen alone or as a part of a syndrome with many other defects. An example is an isolated congenital heart defect. Symptoms of this would be a complete mirror image transportation of the chest and abdominal organs all while the anterior-posterior symmetry is normal. My thoughts on SI are that it’s very amazing how a person could have this genetic condition and be able to still be a perfectly good, live, and breathing

You May Also Find These Documents Helpful

  • Powerful Essays

    Sq3r Chapter 13

    • 1466 Words
    • 6 Pages

    7) Genetic disorders are borne when a variation in the DNA sequence occurs when a single nucleotide in the genome is altered is called single nucleotide polymorphisms or SNPs.…

    • 1466 Words
    • 6 Pages
    Powerful Essays
  • Powerful Essays

    Pt1420 Final Exam

    • 3892 Words
    • 16 Pages

    - caused by a MECP2 mutation. This gene is found on a person’s X chromosome…

    • 3892 Words
    • 16 Pages
    Powerful Essays
  • Satisfactory Essays

    CRI DU CHAT SYNDROME WHO DISCOVERED CRI DU CHAT SYNDROME? In 1963, JEROME LEJEUNE described a syndrome consisting of multiple congenital anomalies, mental retardation, microcephaly, abnormal face, and a mewing cry in infants with a deletion of a B group chromosome (Bp-), later identified as 5p- WHAT IS CRI DU CHAT SYNDROME?…

    • 798 Words
    • 4 Pages
    Satisfactory Essays
  • Satisfactory Essays

    They may present with a number of types of congenital heart disease (e.g. atrial septic defect, ventricular septal defect, or patent ductus arteriosus) Children with the syndrome might have a hernia, abnormalities of their urogenital system, malformed kidneys, or undescended testicles if they are male.…

    • 557 Words
    • 3 Pages
    Satisfactory Essays
  • Better Essays

    Ehlers-Danlos Syndrome

    • 819 Words
    • 4 Pages

    Ehlers-Danlos syndrome is a degenerative condition caused by the malformation of collagen within the body. Many different types of Ehlers-Danlos syndrome have been linked to different types of collagen malformation in different tissues. Hypermobility type Ehlers-Danlos syndrome (HT-EDS) is the most common type of Ehlers-Danlos syndrome. HT-EDS is mainly characterized by marked joint instability and mild cutaneous involvement (Castori et al., 2010). Although it is typically considered the least severe form of the disorder, complications, primarily musculoskeletal, can and do occur (Levy, 2004). Subluxations and dislocations are common as is degenerative disk disease (Levy, 2004). Chronic pain, distinct from that associated with acute…

    • 819 Words
    • 4 Pages
    Better Essays
  • Good Essays

    Genetic testing has potential benefits, such as you can see if your chromosomes are positive for a genetic mutation. Test results can provide a sense of relief from uncertainty about having a mentally or physical ill child because no one wants that for your child. They also help people make informed decisions about managing their health care. For example, a negative result for the mutation can eliminate the need for unnecessary checkups and screening tests in some cases. A positive result, having the mutation, can direct a person toward available prevention, monitoring, and treatment options. Some test results can also help people make decisions about having children. Newborn screening can identify genetic disorders early in life so treatment can be started as early as possible.…

    • 632 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Unit 27

    • 930 Words
    • 4 Pages

    Genetic factors are things you are born with, this happens when a child’s genetic make-up goes wrong examples of genetic factors are Down syndrome and autism.…

    • 930 Words
    • 4 Pages
    Good Essays
  • Good Essays

    When a person is born, their DNA is subject to many different mutations throughout their life. Some of which are inherited from their parents, they develop at birth or during their adulthood. Some of these mutations are harmless and can go unnoticed for your whole existence, while others can alter your health drastically. There are some mutations that are considered to be valuable, as well as a silent one which does not affect you at all. The mutations heard about most often are those that cause disease such as, cystic fibrosis, sickle cell disease, and Tay-Sachs disease (Genetics.) These specific diseases are both devastating and life changing. Each disease is caused by a mutation in different gene and in turn affects different parts…

    • 955 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Muscular dystrophy is a genetic disorder. It is inherited just like height and eye color. Scientists now know that a defective gene causes each type of muscular dystrophy. In…

    • 1466 Words
    • 6 Pages
    Good Essays
  • Good Essays

    9 Months That Made You

    • 565 Words
    • 3 Pages

    In the first case, Melanie Gaydos, from New York, was born with a genetic condition called ectodermal dysplasia. Ectodermal Dysplasia is a genetic condition that develops when clumps of cells become specialized cells, but in Melanie's case, her cells didn't do that. When the different layers of cells…

    • 565 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Genetic testing is being used in the medical field to decrease dangers in patients. The negative connotations brought by these examinations might be the reason a person, whom may have had great talents, will lower their capacity to excel. Insurance companies grant pensions and healthcare, consequently if a person were to be diagnosed even with a minimal chance of cancer by…

    • 478 Words
    • 2 Pages
    Good Essays
  • Good Essays

    mcfarland

    • 557 Words
    • 3 Pages

    One unpleasant aspect of genetic disease is that often they come unexpectedly and with little warning. A few summers ago, my little sister [Lisa]’s face began to undergo a startling metamorphosis. Her skin, once bronze and glistening, began turning white as death and splotchy. My sister’s precious forehead, hair and eyelids began to look like a pale jigsaw puzzle, interrupting her once perfect complexion. This genetic disorder, vitiligo, has permanently changed her appearance and her daily life. I looked on angrily, frustrated by my helplessness, as doctors prescribed her various treatment creams, but offered no cure. My love for my little sister and unrelenting wish for her happiness fueled me to seek the source of her problem – which lies in genetic research.…

    • 557 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    family medical history). Family medical history is included in the definition of genetic information because it is often used to determine whether someone has an increased risk of getting a disease, disorder, or condition in the future. Genetic information also includes an individual's request for, or receipt of, genetic services, or the participation in clinical research that includes genetic…

    • 217 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Unit 18 Babies Development

    • 3936 Words
    • 16 Pages

    Genetics are also a major factor which may influence the health and development of the baby as some illnesses are inherited through genes. For example babies with Down's syndrome suffer due to a chromosomal abnormality which lead to problems such as heart defects and chest infections.…

    • 3936 Words
    • 16 Pages
    Good Essays
  • Satisfactory Essays

    mutation advantages

    • 163 Words
    • 1 Page

    However for as much as mutations have helped us discover, there is also disadvantages, such as disease. Disease happens due to a mutation and the development of it. Not only disease, but also able to cause genetic disorders, an abnormality now found on their DNA. Abnormalities can range from small mutations in a single gene to the addition of an entire set of chromosomes.…

    • 163 Words
    • 1 Page
    Satisfactory Essays