Klinefelter's Syndrome Research Paper

Turner Syndrome Turner Syndrome occurs in females who lack part or all of their second X chromosome. Their genotype for sex chromosomes is XO. Almost all people (approximately 95%) with Turner Syndrome have a short stature and signs of ovarian failure. It can be treated with hormone therapies.

Eric has a possibility of being sterile because of the hyposecretion of T4 and T3, which can cause sterility (Marieb & Hoehn, 2013, p.607). Eric might also be sterile because of his low testosterone levels. This causes semen volume to decrease, and it can impair erection and ejaculation, leading to sterility (Marieb & Hoehn, 2013, p.1034). 2. Is there anything that they could try to do to stimulate spermatogenesis?

Therefore it comes down to the fact that a person does not agree with their chromosomal configuration. These people usually state that they feel like they are a woman trapped in a man’s body or vise versa. It’s all a matter of a complex series of emotions and it can be argued that scientifically it doesn’t exist because it all

Klinefelter syndrome, also known as ‘47,XXY’ and ‘XXY’ is found in males, this is due to the fact that the host male gets another X chromosome. The image on the right you can see the extra chromosome with the pair of sex chromosomes. Usually there are only two chromosomes that determine the sex, one from opposite sexes but when it comes to Klinefelters Syndrome there is an extra X chromosome. Because this due to the additional chromosome it can described as a chromosome disorder. The frequency of getting affect by Klinefelter syndrome is 1in 500 to 1,000 newborn males. Klinefelter syndrome isn’t inherited but occurs as random event during the formation of reproductive cells in a parent. SYMPTOMS AT BIRTH AND CHILDHOOD Birth: Small Penis Undescended Most people with the syndrome are not diagnosed until they are adults but sign of the syndrome show up as you grow to become an adult. If they are early dragonised they can receive help to overcome any problems that are caused by Klinefelter Syndrome KLINEFELTER SYNDROME SYMPTOMS DIAGRAMS GENETICS OF THE DISEASE While Klinefelter Syndrome is a genetic disorder it isn’t inherited by any of the male and female counter parts. This is caused by the additional X chromosome which is can described as an error in cell division called meiosis causes an reproductive cell to have abnormal number of chromosomes. The image on the right clearly shows the karyotype for Klinefelter syndrome and were the chromosome disorder is. Klinefelter syndrome is a chromosomal mutation due to the extra sex chromosome. It is a chromosomal disorder but is still due to the fact that it is random event. GENETICS OF THE DISEASE The additional X chromosome I found with the other two sex chromosomes making it a total of 47 chromosomes instead of 46 which leads to the male child's hormonal and sexual related abnormalities as the grow up. Klinefelter syndrome can be diagnosed through a physical examination, chromosome analysis, blood test and semen

The cause is passed down from mother to son through the X link chromosome making this disease affect the male child.

Noonan Syndrome Having a family member or child with an uncommon condition can be pretty extreme. When it comes to these conditions, they are usually some sort of mutation or run in the family 's genetics. Noonan Syndrome is a rare condition that affects an individual 's physical appearance, mental state, and genetic makeup, but varies in each affected person. In 1963, Noonan Syndrome was first described by a heart-specialist, Jacqueline Noonan.

Treacher Collins Syndrome. In short it's the ugly disease. It made the misaligned outer corners of one's eyes droop down like the leaves of a palm tree. It made one's smile lopsided and more crooked than a witch's nose.

FRAGILE X SYNDROME: A COMMON UNKNOWN GENE Everyday day babies are born with disabilities. A majority of these are surprises to the new parents. Conditions such as: Down Syndrome, sensory impairments and neurological disorders are known to most people but still not anticipated. Fragile X Syndrome is a gene mutation that affects thousands of people, making it important to know how the disorder changes the social and emotional aspects of a person’s development and life.

Rett Syndrome, a rare, non-inherited, genetic, neurodevelopmental disorder. It exclusively affects girls as young as six months. An Austrian doctor by the name of Andreas Rett originally described the disorder in a journal article in the year 1966. The disorder was not recognized as a disorder until the year 1983, when a Swedish researcher by the name of Dr. Bengt Hagberg published the disorder.

In 1866, John Langdon Down, a British physician, identified a group of people whose symptoms were very similar. These were: eyes that were upwardly slanting, a flattened back of the head, and fissured and poorly controlled tongues. The term “mongolism” was coined to describe these people with Down’s Syndrome. In 1959, Jerome Lejeune identified the disorder as a chromosomal condition. He saw that those with the condition had 47 chromosomes in their cells instead of the normal 46.

Sotos Syndrome, Pediatric Sotos syndrome is a condition that causes a child to grow more quickly than other children. Children are born with this condition. Increased growth starts in the womb and may continue until the child is 4 years old. Your baby may be larger and heavier than other infants at birth and, during childhood, your child may be taller and heavier than other children. Many children with Sotos syndrome also have some delay in mental development.

Of course with each option there will never be a 100 percent guaranteed of pregnancy taking place. I feel it’s important to have conversations with both parents about not only about the procedures, but the psychological effects that infertility treatments can have in the long run for both parents. As a social worker discussing infernality treatments with a family can certainly be challenging in many ways. I feel that it’s important to be mindful, and supportive of the decision making process. Offering guidance to both parents is something a social worker can do to help sort through the many options couples may have.

Castleman’s Disease Immune System Castleman’s disease, also known as giant lymph node hyperplasia and CD, is a rare disorder that involves an overgrowth of cells in your body’s lymphatic system. It was first described by Dr. Benjamin Castleman in 1950. CD is not a form of cancer but is called lymphoproliferative disorder, which means there is an abnormal growth of lymphatic cells and is similar to cancers of the immune system. Although it may not be a type of cancer one of the two forms, called multicentric Castleman’s disease, acts just like lymphoma. Many people with multicentric Castleman’s disease actually develop lymphomas.

Imagine wanting to have a baby and not being able to conceive one. Invitrofertilization is the opportunity you've been waiting for it allows same sex couples and single women able to have their own biological children. Invitrofertilization is an emerging issue in the medical field due to infertility of couples, debatable stem cell research, the demanding process, and the outcome of these children. People who cannot conceive a child are not completely out of luck. They have a handful of options, their best option is invitrofertilization.

Walking Corpse Syndrome which is also known as Cotard’s Syndrome is when an individual has an overwhelming feeling that they are either completely dead, or parts of their bodies are missing. This is an extremely rare disease that doesn’t occur in a lot of people. There are also a lot of people who have had it that do not like talking about it, but there was a case in Alabama where a young female had Cotard’s Syndrome and she was brave enough to talk about it. Cotard’s Syndrome is something that happens in the amygdala of the brain which controls a lot of the “feelings” a human receives. This syndrome was founded back in 1880 by a French neurologist named Jules Cotard. This syndrome dates back to 1788 when conditions were first seen, but it