A report on the turner syndrome

On the other hand, predictability is also a curse for both newspapers and television stations.

Turner syndrome and hearing loss

This hearing loss usually resolves as a child ages and ear infections become less frequent. Causes Turner syndrome is caused by partial or complete loss monosomy of one of the X chromosomes.

However, learning difficulties are common among women with Turner syndrome, particularly a specific difficulty in perceiving spatial relationships, such as nonverbal learning disorder.

Affected females may also be prone to infections of the middle ear otitis mediaespecially during infancy and early childhood. A woman with TS has a significantly higher risk of developing complications during pregnancy, including gestational diabetes, high blood pressure, and aortic dissection.

In some cases, affected individuals may begin to undergo breast development and may begin menstruating without therapy spontaneous pubertal developmentbut most will stop developing sexually and stop menstruating at some later point during their teen-age years. Gastrointestinal problems including feeding difficulties and gastroesophageal reflux GERD may also occur.

Men have one X and one Y chromosome in their cells while females have two X chromosomes. Cause[ edit ] Turner syndrome is caused by the absence of one complete or partial copy of the X chromosome in some or all the cells. Kidney renal abnormalities may occur in some cases including horseshoe kidneys or absence agenesis of a kidney.

Turner syndrome may be diagnosed before birth or shortly after birth or during early childhood. Ear infections and hearing loss High waist-to-hip ratio the hips are not much bigger than the waist Attention deficit hyperactivity disorder problems with concentration, memory, attention with hyperactivity seen mostly in childhood and adolescence Nonverbal learning disability problems with maths, social skills, and spatial relations Other features may include a small lower jaw micrognathiacubitus valgus[13] soft upturned nails, palmar crease, and drooping eyelids.

What's to know about Turner syndrome?

Some individuals with Turner syndrome may have multiple tiny colored spots pigmented nevi on the skin. As more women with Turner syndrome complete pregnancy thanks to modern techniques to treat infertility, it has to be noted that pregnancy may be a risk of cardiovascular complications for the mother.

If untreated, severe cases can result in insufficient blood flow to the organs of the body or eventually progress to congestive heart failure. In some cases, the disorder is diagnosed before birth or shortly after birth.

An underactive thyroid gland affects 10 percent of among patients with TS. Kidney abnormalities increase the risk of urinary tract infections and high blood pressure hypertension.

Chromosomes are found in the nucleus of all body cells. Nonetheless, the aortic root diameters found in Turner syndrome patients were still well within the limits. The reason that this occurs is unknown and is believed to result from a random event. Congenital heart defects may be associated with Turner syndrome, especially in individuals with lymphedema.

Report of a case of Turner's syndrome with localized aggressive periodontitis

Especially in mosaic cases of Turner syndrome that contains Y-chromosome e. TS increases the risk of having problems with self-esteem, anxietydepressionattention deficit hyperactivity disorder ADHDand social interaction.

On physical examination, it was seen that the patient was of short stature and had webbed neck with a low hair line at the back of the neck.

Common symptoms include short stature and premature ovarian failure, which can result in the failure to attain puberty. Genetic counseling may be of benefit for affected individuals and their families. In these cases, the loss of genetic material from the X chromosome usually occurs because of spontaneous errors very early during fetal development.

In some cases, the disorder is diagnosed before birth or shortly after birth. However, in some cases, the disorder may not be diagnosed until well into adulthood, often as an incidental finding.

I would prefer not to have to write any. She had been born smoothly without abnormal birth history.

Turner syndrome

Turner syndrome is being increasingly diagnosed before birth prenatally based on chromosomal analysis performed subsequent to amniocentesis or chorionic villus sampling CVS. Affected individuals should also undergo thyroid function tests because of the potential for thyroid disease.

This may also manifest itself as a difficulty with motor control or with mathematics.Parents of girls who don’t appear to be developing at the same rate as their peers and who suffer from frequent ear infections may want to ask their family doctor if she should be tested for Turner syndrome, a rare genetic condition which affects one out of every 2, - 4, female births.

Early diagnosis is key, as those affected have higher incidences of heart, liver and kidney abnormalities, autoimmune.

Turner Syndrome Market

rows · Jul 13,  · Turner syndrome is a chromosomal disorder that affects development in. Table 1. Table 1. Major Clinical Features of Turner's Syndrome. Turner's syndrome, a disorder in females characterized by the absence of all or part of a normal second sex chromosome, leads to a.

The Turner Syndrome Society offers education and support for all those touched by TS. The Turner Syndrome Society offers education and support for all those touched by TS.

Report of a case of Turner's syndrome with localized aggressive periodontitis

Dec 26,  · Turner's syndrome is a disorder in females characterized by the absence of all or part of a normal second sex chromosome. It is typically characterized by the combination of physical features and cytogenetics in females.

In Europe, it is often called Ullrich–Turner syndrome or even Bonnevie–Ullrich–Turner syndrome to acknowledge that earlier cases had also been described by European doctors. The first published report of a female with a 45,X karyotype was in by Dr. Charles Ford and colleagues in Harwell, Oxfordshire, and Guy's Hospital in London.

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A report on the turner syndrome
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