Gender Roles : Gender And Sexuality

I never heard of anyone having a sex chromosomal abnormality. Klinefelter syndrome is a rare condition in males that is caused by an extra X sex chromosome. Males with the XXY chromosome pattern do not develop secondary sex characteristics. Males with Klinefelter syndrome have weaker muscles and may develop breast tissue. They are also infertile because they do not produce sperm. Turner syndrome occurs in females and is caused by having only one X sex chromosome. Most females with Turner syndrome do not produce estrogen and progesterone. This causes poorly developed breasts, no onset of menstrual periods, and possible infertility. However, a woman with Turner syndrome can usually carry a baby to term if another woman donates an ovum and it is fertilized in a laboratory dish and implanted inside

Turner syndrome results in a monosomie of chromosome X and is the only viable monosomie known. One in every 5,000 newborns can inherit this disease. The mental abilities are not affected, although they are usually sterile owing to underdeveloped sex

Normally males have 46 chromosomes which include one X and one Y chromosomes, but males with XYY Syndrome have 47 chromosomes, two of which are Y chromosomes. Most cases of XYY Syndrome occur before conception due to a cell division error in the sperm. Rarely does the cell division error happen after conception.

Disorders of sex development (DSD) are cases where there is a discordance of genetic sex and internal and/or external sex organs at birth related to suppression of, or overexposure to sex hormones in utero. DSDs can also stem from insensitivity to androgens. When these hormonal abnormalities occur, the best general description is that either internal or external genitalia do not form or do not form correctly. In some cases, for example, female genitalia may have a more masculine appearance or the girl may present with both male and female external genitalia, but no internal components such as a uterus (Helgeson, 2012). Wisniewski specifies that study of DSD has provided a greater understanding and appreciation of the impact of hormones on behavior, which has in part caused a reassessment of DSD-related treatments. However, she also emphasizes that socialization and learning have significant influence on gender and gender-role development, but only when prenatal androgen exposure is not a factor. Wisniewski added that she would like to see a gender marker that could be identified from birth and used as part of the formula for predicting gender development. Unfortunately, her own research demonstrates far too much societal and cultural involvement in gender and gender-role development

It is not a very common disorder, but one factor that can contribute to this condition is when a woman over the age of 35 gives birth. As a woman ages so do her eggs. The genetic information inside the egg has a greater chance of being altered. Mutations and nondisjunction are more likely to occur in older eggs. Doctors have found that this disorder is really caused by random chance of a problem that occurs during meiosis. Parents of a Klinefelter boy are not to blame for their son having this condition.

Starting at the time of the usual onset of puberty, testosterone replacement can help treat or prevent a number of problems. Testosterone may be given as an injection or with a gel or patch on the skin. The therapy allows a boy to undergo the body changes that normally occur at puberty, such as developing a deeper voice, growing facial and body hair, and increasing muscle mass and penis size. It can also improve bone density and reduce the risk of fractures. It will not result in testicle enlargement or improve infertility. Breast tissue removal in males who develop enlarged breasts (gynecomastia), excess breast tissue can be removed by a plastic surgeon, leaving a more normal-looking chest. Speech and physical therapy treatments can help boys with Klinefelter syndrome overcome problems with speech, language and muscle weakness. Educational support is very important with boys who have Klinefelter syndrome. They usually have trouble learning and can benefit from extra assistance. Parents should talk to their child's teacher, school counselor or school nurse about what kind of support might help. Most men with Klinefelter syndrome are unable to father children, because no sperm are produced in the testicles. Some men with Klinefelter syndrome may have some minimal sperm production. One option that may benefit men with

An example of a recessive x-linked disorder is fragile x-syndrome or FXS. Fragile x-syndrome affects a person’s behavior, learning, intellectual, as well as physical characteristics. Fragile x-syndrome is more likely to affect males over females and does not shorten their life expectancy. Males who have FXS can have ADD or ADHD, autism, aggression and other behavioral traits. Men can have physical alterations such as a long face, large ears, and flat feet. Women who have FXS can experience the same behavioral traits but are usually milder in comparison to men. The same is shown through the facial features for women (National Fragile X Foundation,

Through examining the ways intersex individuals are treated in a medical setting, one can see how science only allows binary bodies to be created. Crawley et al. (2007) discusses intersex individuals and the standard treatment of intersex children, being to alter their ‘abnormal’ genitalia to resemble one of the two genders. This has become the normal treatment as if this is necessary, but the only threat the child is in danger of is not fitting perfectly into the heteronormative standard of correct genitalia. Because surgical intervention proves we alter and change one’s sex, it becomes difficult to claim that sex and gender are solely biological, when clearly one’s gender and sex becomes largely altered the moment they are born into society. Anne Fausto Sterling, outlines her concept of the five sexes, explaining that intersex is a term used to describe any individual that doesn’t fit into the narrow categories of male and female. She explains that the same process that was in play in the Middle Ages is

Discovered in 1938 by Dr. Henry Turner, Turner’s Syndrome is where a female is born with either a x-chromosome missing, or the chromosome being altered in some way. Signs a girl has this disorder can include: puffy feet and hands at birth, short stature, low growth hormone levels, and a delay in puberty. Turner’s is rare, as it occurs in about one in every 2000 births. I was that one birth. Pediatric Endocrinologist Nancy Wright is the one who diagnosed me with it on October 11, 2014. The day was a fall day, with the crunchy leaves on the sidewalk and the doorway. That day was also a little cold. Not too cold, but not burning hot either. The ride took about an hour from my home state of Georgia, to Dr. Wright’s office in Tallahassee, Florida.

Turner Syndrome is caused by a missing or incomplete X chromosome. People who have Turner Syndrome develop as females. Some of the genes on the X chromosome are involved in the growth of your height and sexual development, which is why girls with this disorder are shorter than normal and have incompletely developed sexual characteristics. Within this disorder there can be many symptoms, for example: swelling hands and feet, heart defeat, pregnancy chorionic villus sampling or amniocentesis. There are also major causes contributing to this disorder including a stocky build, arms that turn out slightly at the elbow, receding low jaw, a short webbed neck and low hair line on the back of the neck. Also includes backtracked puberty, ovaries undeveloped properly and effects sexual development.

Men with this condition have longer legs, a higher voice, and a thinner beard than average men do. Their testicles are smaller than usual and do not produce functioning sperm cells, so the men are infertile. Compared with other men, they have lower levels of androgens (male hormones) and more estrogens (female hormones). For this reason, they often develop gynecomastia (benign male breast growth) and have an increased risk of male breast cancer.

In 1938, Dr. Henry Turner first described Turner Syndrome. Turner Syndrome a genetic disease that only affects girls, in fact, it is one of the most common sexual development disorders (Radtke et al. 2014). It is caused by an abnormal sex chromosome, either an abnormal X chromosome or a missing X chromosome. The sex chromosome contributed by the father to the child determines the sex of the child because the mother always contributes an X chromosome whereas the father can contribute either an X chromosome or a Y chromosome (Snustad 2012). Turner Syndrome is the result of an abnormal sex chromosome, so if the father’s sex chromosome is missing, then the child will only have a single X chromosome from the mother resulting in the child being

Normally, a female inherits one X chromosome from each of her parents. However, girls with Turner syndrome do not have two complete X chromosomes. Approximately half of individuals with Turner syndrome have monosomy X, which means each body cell has only one copy of the

The XXY syndrome, most commonly known as Klinefelter syndrome (KS), only affects males of all ages. This syndrome occurs when there is a random genetic error after conception and is not curable, however treatment can help.All females have XX chromosome and all males have XY chromosomes. Unlike the normal XY type that all males have, males affected have an additional X chromosome which results into many symptoms such as impaired spermatogenesis, low testosterone, and male hypogonadism. Since Klinefelter syndrome is related to the sex chromosomes of males, it is a sex link trait.

People typically have two sex chromosomes in each cell: females having two X chromosomes, while males have one X chromosome and one Y chromosome. Turner syndrome results when one normal X chromosome is present in a female's cells and the other sex chromosome is missing or structurally altered. The missing genetic material affects development before and after birth. About half of individuals with Turner syndrome have monosomy X, which means each cell in the individual's body has only one copy of the X chromosome instead of the usual two sex chromosomes. Turner syndrome can also occur if one of the sex chromosomes is partially missing or rearranged rather than completely absent. Some women with Turner syndrome have a chromosomal change in only some of their cells, which is known as mosaicism. This type of Turner syndrome may result milder symptoms than other types of the disorder. In order to diagnose mosaic Turner syndrome, healthcare professionals may examine blood cells and/or skin