ipl-logo

Klinefelter's Syndrome Research Paper

797 Words4 Pages

In 1942, Dr. Harry Klinefelter and his team first identified the combination of features that are now known as Klinefelter Syndrome (KS).1 By the late 1950s, a group of researchers deduced that men with those features had one extra X chromosome. Although KS is the most common sex-chromosome abnormality, the amount of famous people who identify with this disorder are limited. However, some examples would be Lili Elbe, a transgender Danish painter/model, and George Washington, the first President of the United States. Even though the symptoms of Klinefelter Syndrome may vary depending on the individual, some common signs are: delayed or incomplete puberty, reduced muscle mass, breast enlargement (gynecomastia), reduced hair, infertility (little …show more content…

While it increases energy, strength, and sex drive, this therapy also promotes growth of body hair, improves appearance of muscles, ability to concentrate and helps maintain mood and self-esteem.10 Another type of treatment would be therapy for speech, behavior, and/or physique, which can improve speech impairments, academic difficulties, and other psychosocial and behavioral problems.10 Starting at a young age, these therapies may help children understand/produce more complex language, and improve muscle tone, balance, and coordination.10 Fertility treatment, more specifically intracytoplasmic sperm injection (ICSI) may also be chosen as an option.10 Since most men are unable to father children because there is little to no sperm in their testicles, sperm can be removed from the testicle with a biopsy needle and injected directly into the egg. If that fails, they can also choose adoption or artificial insemination with donor sperm.10 Even though there are many other treatment options available to help individuals cope with KS, the last example of a

Show More
Related
852 Words | 4 Pages

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.

Read More
1100 Words | 5 Pages

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?

Read More
733 Words | 3 Pages

Of course, the condition will most likely involve a heart problem, which is discovered at birth, along with a webbed neck, chest deformities, many birth marks, also known as café-au-lait spots, and a short stature. The features of this syndrome are not fully known, considering the fact that there are numerous characteristics and no two infected individuals have the same exact features. Like in most other disease cases, there are lists of more minor symptoms that can occur in an individual. In infants and newborns, feeding problems are present, due to a poor sucking reflex. Behavioral problems and developmental delays can occur, which causes the individual to achieve milestones slower, such as sitting and walking.

Read More
440 Words | 2 Pages

Name: Horner 's syndrome Overview: The syndrome of Horner is a neuro-ophthalmological that develops after an interruption of nerve fibers nice ranging from the hypothalamus to eye. Possible damage to the central level that causes this syndrome is the lesion, compression or ischemia of the brain stem. Other conditions that determine the Horner syndrome is syringomyelia and some cancers marrow or brain (eg. neuroblastoma). Interruptions devices, however, can result from head and neck trauma, cervical lymphadenopathy, lung tumors Pancoast, aortic dissection or carotid artery and thoracic aortic aneurysm.

Read More
1274 Words | 6 Pages

Medi-Cult Case Analysis Medi-Cult, a biotech company based in Denmark, has developed a new alternative to In Vitro Fertilization (IVF) called In Vitro Maturation (IVM). These methods are used to help infertile couples have children. IVM significantly reduces the time needed to mature an egg from 30 days to just 2 days. Importantly, it is a relatively hormone-free treatment thus sparing women a number of psychological and physical side effects. Because the side-effects tend to be much-lessened, women at risk from hormone-related condition such as polycystic ovaries are offered the option of safer fertility treatment.

Read More
270 Words | 2 Pages

Parry-Romberg Syndrome Parry-Romberg syndrome is an uncommon disease that slows the progressive deterioration of the skin and soft tissues in half of the face. This disease usually affects the left side of the face. The disease is more common to happen to females than males. Some signs that you have this disease are facial changes by the upper jaw, between the nose and upper corner of the lip, change in the angle of the mouth, eyes, brow, ear, and neck. This can also affect the tongue, roof of the mouth, and the gums.

Read More
790 Words | 4 Pages

Stevens Johnson Syndrome Stevens Johnson syndrome is a serious condition that affects the skin and external linings (mucus membranes) of the body. It is usually associated with an abnormal response to some medicine you may have been taking for a few days, but fortunately, it is a rare condition. Common medicines that can cause Stevens Johnson syndrome include antibiotics, pain killers, and anticonvulsants. Part 1: Symptoms of Stevens Johnson Syndrome (SJS)

Read More
670 Words | 3 Pages

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.

Read More
612 Words | 3 Pages

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.

Read More
570 Words | 3 Pages

Addison’s Disease is a rare disorder where the adrenal glands, that’s located directly above the kidney, does not produce enough of the cortisol hormone. Addison’s disease can be separated into 2 sub conditions, primary adrenal insufficiency and secondary adrenal insufficiency. People with primary adrenal insufficiency suffer from both a lack of the aldosterone hormone and the cortisol hormone the adrenal glands produce. People with secondary adrenal insufficiency only suffers with a lack of cortisol. The disease is found in every age group and both sexes.

Read More
1071 Words | 5 Pages

Should cheerleading be considered a sport? Absolutely! I love the sandbox! “Cheer encompasses many different aspects - - - from physicality to showmanship” (Gray).Cheer is an activity that involves physical exertion and skill (Gray).“The skill cheerleaders have such as routines that require one or two people to lift their body weight, if not more, in the air quickly and with precision. ”(Gray).“Cheerleading is competitive, with athletic requirements rivaling those of other team sports”(Bennett).

Read More
691 Words | 3 Pages

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.

Read More
1013 Words | 5 Pages

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.

Read More
1683 Words | 7 Pages

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.

Read More
1042 Words | 5 Pages

Everyone is entitled to choose their own lifestyle, whether they want to have a child or not. Some females who seek to have children find it easy, although some are unfortunate. There are numerous of reasonings, such as being too old to be pregnant, damage to the Fallopian tube or uterus and cancer radiation or chemotherapy. As our generation goes on, many discoveries revolving biology is produced and one of it is the In Vitro Fertilization or “IVF”. It is the procedure of fertilization where they save sperm sample, take an egg from the women and physically combining it in a laboratory dish where the egg and the sperm is now called an embryo.

Read More

More about Klinefelter's Syndrome Research Paper

Related Topics

Open Document