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Genetic mutation and disorders essay
Genetic mutation and disorders essay
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The study of genetics includes not only the study of normal DNA, but also of the mutations within a DNA. A mutation is a slightly distorted gene. These mutations can have an effect on a person, both physically and mentally. Although genetics may seem to be just about the genes, scientists are beginning to see a connection between gender and genetic mutations.
Meet Henry, a man with dark hair, and Katie, a woman with gapped teeth. The couple has a child and from their physical description, we know that the child may turn out to have dark hair and gapped teeth. These simple examples are what color the fundamentals of genetics, but what if Henry and Katie have twin children. One child is a girl and she has dark hair and gapped teeth. She is normal and has no conditions or problems. The other child is a boy. The boy, like his twin sister, has dark hair and gapped teeth, but, unlike his sister, begins to show signs of autism at the age of three. Neither Henry nor Katie has autism, yet their son does. After some genetic testing, the doctors find that Katie’s great-grandfather did have autism and Katie was a carrier, or she had the gene for autism, but the gene was recessive, or inactive. Why, though, in Katie’s son, was the gene active instead of recessive? Why did it not affect the daughter? This question is one that puzzles everyone. It could have been a coincidence that the son developed autism and the daughter did not. If it was just a coincidence, then why is it that one in every 88 U.S. children will develop some form of autism, but boys develop autism 4 times the rate seen in girls? Is there more to genetic mutations than we think? Could there possibly be a connection between gender and genetic...
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...ry and Katie’s son inherited the autism was because, as a boy, he was much more vulnerable to the disorder. Through much study, many scientists would agree that it was not the boy’s genes, but the male genes inside of him that caused him to react to the autism gene. This has no effect, though, on him leading a normal life. As studies continue to go on, perhaps we will one day find out why males are more vulnerable to many genetic conditions. Through many more years of research, medical trials, and genetic testing, we may finally find out the connection between gender and genetics.
Works Cited
Sanders, Laura. Why Boys Face Higher Autism Risk. 5 March 2014. 24 March 2014 .
The National Autistic Society. Autism: Why do More Boys than Girls Develop it? 14 March 2014 .
exercises that will benefit the life of the child. However, not every parent is able to deliver a healthy child because the genetic mutation and diseases that cause the child die before birth or at a very young age. With the advancement in biotechnology, genetic engineering will be able to make the offspring of these parents healthy. According to dictionary.reference.com genetic engineering is the deliberate modification of the characteristic of
must contain either the BRCA1 or BRCA2 gene mutation in her genetic make up. Hundreds of mutations have been found in both genes and almost all of the mutations identified are primitive mutations found in only a single family. Most of the mutations result in a miss-formed protein product; thus the nature of these mutations is easily interpreted. Two successive acquired mutations occurring in a single cell are necessary for the development of cancer. Mutations anywhere along either gene are associated
Genetic engineering is the modification of an organism’s genes, to achieve a desired product. It is a likely possibility that in the future, this process will be used on humans. Many people think that genetic engineering is a good idea, but they are wrong because it can lead to even stronger mutations and will erase individuality. Multiple people think that there are many advantages to genetic engineering. First of all, it can help to prevent and eliminate genetic disorders (Hanson). Some diseases
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nurture (environment) and nature (genes). The nature vs nurture is a scientific, cultural, and philosophical debate about whether human culture, behavior, and personality are caused mainly by nature or nurture. Nature in this debate is referred to as genetic or hormone-based behaviors. Nurture in the argument is referred to as environment and experience. A big issue in developmental psychology is the connection between .the innateness of an attribute (if it is apart of our nature) and the environmental
Genetic engineering is the “science of altering and cloning genes” to treat diseases but it can also branch out to the creation of designer babies or human modification according to Dictionary.com. DNA faulty is said to be the “major causes of death and disability, including cancer, heart disease, Alzheimer’s disease and diabetes” (Merz). People deem the practice of genetic engineering as a breakthrough for humans because of the possibility of humans cure of cancer or diseases. This is an accomplishment
every 15,000 to one in 40,000 live births. Achondroplasia is caused by a gene alteration (mutation) in the FGFR3 gene. The FGFR3 gene makes a protein called fibroblast growth factor receptor 3 that is involved in converting cartilage to bone. FGFR3 is the only gene known to be associated with achondroplasia. All people who have only a single copy of the normal FGFR3 gene and a single copy of the FGFR3 gene mutation have achondroplasia.” (genome.gov) Description: Most dwarfing conditions are described
Genetic Mutation in America America has been introducing foreign genes into cows, mice, sheep, and pigs for years; there is no reason that it cannot be done in humans as well (“Creating Designer Children”). Imagine parents picking their child out of a catalog instead of using God’s creation. (“Creating Designer Children”). Every child is born with the genes that are carried down the gene line of their family not by the parents picking how they want their child to be born. Genetic mutation is basically
Summary Sharon Moalem, the author of Inheritance, is a geneticist who through the penning of this novel, effectively educated readers in the field of genetics and revealed connections between inheritance and epigenetics. Throughout the novel, He used several distinct phenomena to illustrate the importance of what people inherit and how life experience can change genes. He shows readers the importance of what they inherit by showing how what you inherit can help or hurt you. The first example
because of their genetic makeup which could lead to a breakdown in communication between the patient and the doctor (Cuticaaa, et al., 2014). There is also a privacy issue in that the patient’s genomic profile may be stored on a database for research uses and some patients may not want their DNA profile for anyone to see if it’s not for the purpose of their own treatment (Caplan, 2016). Patients may also find out things they would not want to. For example, if comparing the genetic profiles of family
changed by ‘chance.’ The preconceived notion that evolution is completely based on chance is invalid. While chance and genetic variation are components of the process of evolution, other selective mechanisms play a large part to help organisms adapt and survive (“Mechanisms of Change” n.d.). Contrary to the belief that natural selection in evolution is mostly a random process, genetic traits that help benefit certain species are most likely to be chosen rather than malignant traits, causing the entire
passed on to future generations certainly would be tempting for many people. A method by which we could prevent genetic diseases and customize our offspring’s gender, physical traits and the intelligence is not as impossible as it may seem at first. The debate over the designer children revived recently with the discovery of the new technique allowing scientists to alter DNA. Genetic engineering was originally designated for medical purposes to correct the mistakes in DNA that condition certain
Osteogenesis Imperfecta (OI) is a disease that is commonly referred to as brittle bone disease. Children with OI tend to have more fragile bones than children who are not affected and are very susceptible to bone fractures. With the correct support and proper management, the patient and their family can live relatively normal and happy lives. Nutrition, exercise, and maintaining a healthy weight are extremely important factors in controlling the factors and symptoms related to OI. Bone health is
ventricular tachycardia (Antzelevitch 2016). According to Genetic Home Reference this can be cause by a mutation in one of several genes, the most common being SCN5A. This gene is responsible for providing the instructions that make a sodium channel within the cell. This channel would normally move positively charged sodium ions into the hearts muscle cells which is imperative for maintaining a healthy, normal heart rhythm. A mutation in this gene can change the function or structure of this channel
significantly caused in people by de novo mutation, deletions, duplications, genomic rearrangements, or point mutations in the germ line of one parent that causes loss of function or gain of function to a large number of genes. This can occur in any family with any genetic background and can appear in any offspring, regardless of gender. Offspring’s with mild disorders (asymptomatic carriers) i.e., females may marry and have children who inherit mutations in a dominant way. It is now obvious that