Turner Syndrome And The Age Of Puberty - 1018 Words

Turner Syndrome Introduction Turner Syndrome is a disorder that affects one in every two thousand girls. Usually girls are born with only one X chromosomes. Some are born with an extra chromosome, or sometimes even half of one is missing which causes Turner Syndrome. Symptoms of Turner Syndrome Most of the girls that have Turner Syndrome are way shorter than average girls. The girls often have their normal height up to three years old. After they are three the growth rate starts to slow down. Ovaries that are non-functioning are other symptoms of Turner Syndrome. A girl’s ovaries begin to produce sex hormones at puberty. This doesn’t happen with most girls who have Turner Syndrome. Most don’t start their periods or develop breast†¦show more content†¦Diagnosing Turner Syndrome Usually the girls with TS are diagnosed around the time they are born. Or at the time they are expected to go through their period. Usually if a baby girl has the signs of Turner Syndrome, a doctor around the hospital will order a special blood test called a karyotype. This test counts the number of chromosomes, this test can also identify any that are abnormally shaped or have some missing pieces. If the blood test shows that a girl has Turn er Syndrome, her doctor may order additional test to check for problems with her kidneys, heart, hearing, and other problems that are often associated with Turner Syndrome. Some diagnosing can be made at birth or close to birth because of heart problems, an unusually wide neck or swelling of the hands and the feet. 2 Turner Syndrome can also be suspected in pregnancy during an ultrasound test. Turner Syndrome during pregnancy can be confirmed by prenatal testing by sampling, or getting cells from the baby for a chromosome analysis. If the diagnosis is confirmed prenatally, also the baby may be under the care of a specialist pediatrician, also the baby may be under the care of a specialist immediately after birth. Noonan s Syndrome is associated with some of the clinical features of Turner Syndrome. Noonan s Syndrome has some of the same usually features, for example short stature, heart defects,Show MoreRelated Turner syndrome Essay1096 Words   |  5 Pagesabnormalities. The Turner Syndrome (known as Ullrich-Turner Syndrome in Germany) is a congenital disease. A German doctor named Ullrich published his article in 1930. American doctor Henry Turner recognized a pattern of short stature and incomplete sexual maturation in otherwise normal females. He published a comprehensive medical description of the syndrome. It was not until 1959, that it became clear the syndrome was due to lack of sex chromosome material. Turners Syndrome is a rare chromosomalRead MoreTurner Syndrome, A Rare Medical Disorder1351 Words   |  6 PagesDysgenesis Gonadal Dysgenesis, also known as turner syndrome, is a rare medical disorder that affects 1 in every 2,500 girls (kidshealth). It is a chromosomal that occurs when one of the two X chromosomes found in females are missing or is incomplete. This condition only affects females. Although researches don’t know exactly what cause turner syndrome, they do know that it’s a problem with a female chromosome. Females who are born with Tuner Syndrome are short in height and effects their sexualRead MoreTurner Syndrome : A Chromosomal Disorder1165 Words   |  5 PagesTurner Syndrome Shinji Lin December 15, 2015 Period 5 Turner syndrome is a chromosomal disorder that affects development in females. This condition is caused by a missing or incomplete X chromosome. In 1938, Henry Turner, an American endocrinologist, described seven women with short stature, lack of sexual development, neck webbing (extra skin on neck), low hairline, and cubitus valgus (arms that turn out at the elbow). Years earlier, Otto Ullrich, a German geneticist, independently describedRead MoreDNA is Everywhere522 Words   |  2 Pageserrors occur then mutations can happen. Turner Syndrome is only found in females. This syndrome is caused by the absence of an X chromosome or the nondisjunction of the X chromosome. This is a chromosomal disorder meaning â€Å"an abnormal condition due to something unusual in an individuals chromosomes.† Turner Syndrome is due to a chromosome mutation rather than a gene mutation. The missing X chromosome affects the development of the female. Usually Turner Syndrome is not inherited from the parent andRead MoreGenetics Synthesis: Marfan Syndrome Essay1514 Words   |  7 PagesMarfan Syndrome Marfan Syndrome is an autosomal dominant disorder mainly caused by defects in the gene FBN1 that codes for the protein fibrillin. Approximately 1 in 5,000 people are affected. Cardinal features involve the ocular, musculoskeletal, and cardiovascular systems. There is a high degree of variability of this disorder, sometimes presenting itself at birth or later in childhood or adulthood. On one end of the spectrum is severe neonatal presentation with rapidly progressive diseaseRead MoreEtiology, Incidence, Clinical Manifestations, And Diagnosis Of This Condition1591 Words   |  7 Pagesmay experience problems with peers, milestones, and adolescence are individuals diagnosed with Turner Syndrome. The purpose of this paper is to explain the etiology, incidence, clinical manifestations, and diagnosis of this condition. Also discussed within this paper will be the current treatments for this condition along with its potential affects within specific areas of development. Turner Syndrome is a genetic condition that affects mainly woman and occurs on the X-chromosome. Instead of havingRead MoreTurner s Syndrome : A Condition That Effects1609 Words   |  7 PagesTurner’s syndrome is a condition that effects 1 in 2,500 newborn girls (Bondy, C.A. 2009). There are many names for this condition including 45 X, TS, Ullrich-Turner syndrome, and Turner syndrome. While females usually have two X chromosomes, these girls are born with only one X chromosome or the second X is altered. While some of the babies make it through full term, some who have this condition are prone to unexpectedly aborting. Diagnosis of the missing or altered chromosome could happen duringRead MoreSymptoms And Treatment Of Celiac Disease1068 Words   |  5 Pagesnon-HLA genes), the enzyme tissue transglutaminase modifies ingested gluten and an abnormal T-cell mediated response occurs in response, leading to initiation of an inflammatory reaction, subsequent intestinal tissue r emodeling and malabsorption syndrome (Koning, 2015 Rostami-Nejad, et al., 2015). This insensitivity differs from food allergies, which are mediated by IgE or IgG (Hill, 2016). Prevalence and Clinical Manifestations CD is one of the most common chronic diseases in children andRead MoreAn Autoimmune Disease : A Common Cause Of Death For Young Women3326 Words   |  14 Pagesk.a. lupus). Both are composed of roughly 85-90% women (Figure 1).1 Autoimmune thyroiditis is one of the most common autoimmune diseases; existing in roughly 1 out of every 200 people.1,3 It is rare in children and most common in women above the age of 60 (~1 in 13).3 Its primary symptom is hypothyroidism. The other autoimmune disease, lupus, is less common; existing in roughly 1 out of every 2,000 people. Its symptoms can include arthritis, rashes, photosensitivity, serositis, oral ulcers,Read MoreSAGHE Case Study1289 Words   |  6 Pagesbe classified and sorted based on demographic variables, sex, age, year of treatment and country. SAGhE study will also extract the additional information in order to provide the most accurate research result based on specialists’ best interpretation of the existing informati on. These information will be including, but not limited to: Birth characteristics, heights, weights, parents’ heights, bone age, GH stimulation test results, puberty status, rhGH dosage and duration of treatment and the initial