Essay on Gender and Genetic Mutations

Although men and women have significant biological differences, the question whether gender-specific labels stems from these biological differences or are gender constructed remains a polarised nature versus nurture debate. Whether it is through the process of socialisation or genetic make-up, “gender identity” is given from a person’s birth, determining how a person culturally interacts and the expectations society places on them. Along with a “gender identity” comes a whole set of “norms”, “values” and so-called “gender characteristics”, which are supposed to define the differences between a male and a female. According to the World Health Organisation (n.d.), the term “sex” is often used to define the biological and physiological

HW: Meta-Analysis- Investigating the genetic and prognostic Sex Differences in Autism Spectrum Disorder. Introduction: While Autism Spectrum disorder (ASD) has been researched extensively, the role of gender in this disease is still poorly understood. With a 4:1 gender distribution in the diagnosis of ASD, many research studies have attempted to explain this difference (Fombonne,2009). Current research has theorized about various different etiologies for this gender discrepancy, such as a female protective effect (Jacquemont et al., 2014). The female protective effect suggests that females must demonstrate higher levels of genetic risk factors in order to reach clinically impaired functional status and therefore be diagnosed (Chawarska,

Genetics can help answer questions about our traits and why we look different and advance in different ways from each other in the world. Chapter 1 explains the basics about how genes work, and the portrayal of DNA and RNA. Chapter 2 describes RNA more in detail and it consist of the explanation of the human genome. Specifically, Chapter 3 clarifies how evolution works and how it relates to genetic and medical research. Furthermore, Chapter 4 and 5 explains the knowledge researchers have about genes role in health and diseases, and how society is affected with the advances in medicine and science given approximate credit to these researchers.

There are many known genetic diseases in the world. There are different types such as chromosomal and monogenic. Chromosomal disorders are when someone has too many or not as many chromosome as they are suppose to have (46 total chromosomes). Chromosomal disorders can also manifest when there are structural abnormalities. Monogenic disorders are an inherited medical condition caused by a DNA abnormalities. These diseases occur all throughout the world today. Depending on what region of the world you are in depends on what the most common ones are. Cystic Fibrosis has become the most common lethal genetic disease in the United States as of 1999. Although there are treatments available, there is not a known cure, and the effects remain burdensome

A very important piece of who we are as humans are genetics. Without genes, we wouldn’t have the same eye color, hair color, nose size, mouth size, freckles, dimples, and many other physical appearances. Not only would we not have the same physical appearances, our brains would be different. Your brain may have diseases that it does not have now. The study of genetics has come a very long way since it was first introduced. Nancy Wexler was an enormous contribute to the study of genetics through personal experiences, the Hereditary Disease Foundation, and her journey in Venezuela.

A mutation is a change or error in an organism’s DNA, while the organism is still developing. The DNA that is replicated is not functional, so the cells follow the wrong set of instructions, which prevents the organism from developing normally. Cells that follow the wrong set of instructions, often leads the organism to growing an extra limb, or the organism may develop a disease/disorder. Some mutations can cause an organism to be missing an important protein. The organism’s proteins are important, they make up mostly the whole organism’s body. Parents with mutations usually pass down their genes to their offspring. Mutations are usually genetic. Environment also plays a role in causing mutations, smoking, sunlight, and radiation are mostly

These mutations can be due to an error in DNA replication or due to environmental factors, such as cigarette smoke and exposure to radiation, which cause changes in the DNA sequence. These changes can affect

There are many biological differences between males and females that cause males to be more susceptible to autism. According to a study performed by Sheryl Ubelacker, males missing one gene called, PTCHD1, on their X chromosome are much more likely to have autism. While females are not affected as noticeably by this because the posses two X chromosomes. Men inherit their X chromosomes from their mothers, indicating that women carriers of this mutation enabling autism (Toronto Star). Having a higher risk for autism does not mean that autism research should be focused on men. It is equally important to find out why women have autism and it could lead to discoveries that would help both males and females. Having a deeper understanding of why women are not equally affected by X chromosomes and why the different affects the Y chromosome has on males and their chances of getting autism is an important research development. Without this knowledge there would still be more questions as to why

A genetic disorder is an illness that is caused by one or multiple abnormalities in the genome. Genetic disorders are not unusual, however when a genetic disorder occurs it usually happens in one and every thousand or million persons. Sometimes genetic disorders can or cannot be heritable, meaning passed down from the parents to their offspring. Often times the parents are unaware that they can carry over a genetic disorder to their offspring. When genetic disorders that does not occur from the parent, it can mean that the cause for the genetic disorder is caused by a new mutation or changes in the DNA. Most cellular structures consist of proteins that carry out to work and to perform life functions. When a gene is disrupted in a way that the proteins no longer carry out a normal function, a disorder can occur.

Approximately three to four percent of babies born every year are born with some kind of genetic disorder. A genetic disorder is described as an illness caused by an error in one’s genome, and is usually hereditary. To understand how these errors occur, one must first understand the basic concept of genes. Genes are the basic units of heredity and are made up of pieces of DNA that instruct the cell how to make specific proteins. Humans are estimated to have about 20,000 to 30,000 genes in their genome. Chromosomes contain these genes and DNA. Humans have 23 pairs of chromosomes or a total of 46 chromosomes. One pair of these chromosomes determines the sex of a person while the other 22 are autosomal, meaning that they determine the rest of

What is a genetic disorder? Scientifically speaking it is defined as a permanent alteration in the DNA sequence that makes up a gene. This alteration could be as small as the addition or deletion of a single base pair or large enough to cover multiple genes.

Genetic disorders or heredity diseases are disorders that are caused by a missing gene, abnormal gene, or chromosomal characteristic (The Free Dictionary, 2007). There are to me found many genetic disorders. Klinefelter syndrome is an example of a genetic disorder. Klinefelter syndrome affects the male rather than female (“47, XXY”, 2016).

Dr. Laura Allen has spent years studying the brain tissue of both boys and girls. She said, "As I began to look at the human brain more and more, I kept finding differences, and about 7 or 8 of the 10 structures that were actually measured turned out to be different between men and women" (Men, Women). Basically, it is best to always try to learn about human nature, that way we can educate people to prevent them from misusing the information. She claims, "knowledge we get is better, we can alter our education system for more equality" (Men, Women).

Then determine the ratios in which each of the character traits is found and also what possible genotypes the parents might be.(stallsmith)

In order to answer the question above this essay will discuss in depth what exactly sex is and what gender is and the differences between the two terms. The research carried out will display that we live in a patriarchal society without a doubt as we look at how gender links to inequality in society. A patriarchal society can be clearly seen from the gender inequality in the labour force which is paid labour and also in unpaid labour which occurs in the household. Another area the answer will reflect on is how gender inequality links to education which overall links to society. Finally the answer below will show how the media also portrays gender inequality and how it affects the people in society.