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When does turners syndrome present itself?
Turner syndrome typically presents itself before birth or during early childhood. Symptoms may include short stature, webbed neck, and primary amenorrhea. Girls with Turner syndrome may also experience infertility and other health issues.
What are characteristics of Turners syndrome?
Depending on the type of Turner syndrome a person has, their karyotype is either: 45X - classic Turner syndrome - second X chromosome missing from all cells 45X/46XX - Mosaic Turner syndrome - second X chromosome missing from some cells. There is another type of Turner syndrome, but it has a more complicated karyotype and I am not sure what the karyotype is off the top of my head.
What conditions are associated with Turner syndrome?
characterized by retarded growth that leads to a small stature and frequent infertility. Individuals with Turner syndrome report an increased incidence of fractures in childhood and osteoporotic fractures in adulthood.
What syndromes is chracterized by karyotype with 45 chromosomes?
Turner syndrome is characterized by a karyotype with 45 chromosomes, including a single X chromosome (X0). This syndrome is associated with short stature, webbed neck, and infertility in individuals with female characteristics.
What are facts about Turner's syndrome?
occurs in about one in every 2500 female childrennot a hereditary disease, neither from environmental or health problems concerning the motherimpossible to conceive children though with help of proper treatment it can be done
Is there any way to predict if a child will have turner's syndrome?
swollen hands and feet wide and webbed neck
When does turners syndrome present itself?
Turner syndrome typically presents itself before birth or during early childhood. Symptoms may include short stature, webbed neck, and primary amenorrhea. Girls with Turner syndrome may also experience infertility and other health issues.
What are some symptoms of turner syndrome?
Symptoms of Turner Syndrome include: short stature, broad chest, low-set ears, sterility, increased weight, amenorrhoea, webbed neck, visual impairments, hearing loss, ADHD, lack of breast development, swelling of hands or feet.
What are characteristics of Turners syndrome?
Depending on the type of Turner syndrome a person has, their karyotype is either: 45X - classic Turner syndrome - second X chromosome missing from all cells 45X/46XX - Mosaic Turner syndrome - second X chromosome missing from some cells. There is another type of Turner syndrome, but it has a more complicated karyotype and I am not sure what the karyotype is off the top of my head.
What conditions are associated with Turner syndrome?
characterized by retarded growth that leads to a small stature and frequent infertility. Individuals with Turner syndrome report an increased incidence of fractures in childhood and osteoporotic fractures in adulthood.
What syndromes is chracterized by karyotype with 45 chromosomes?
Turner syndrome is characterized by a karyotype with 45 chromosomes, including a single X chromosome (X0). This syndrome is associated with short stature, webbed neck, and infertility in individuals with female characteristics.
What are the physical characteristics typical of people with Klippel Feil syndrome?
People with Klippel Feil syndrome are often identified due to three major characteristics: a short neck, a low hairline, and restricted neck mobility due to the fused cervical vertebrae.
How Turner syndrome affects the body?
Summary of what is written below: Women and girls with Turner syndrome are shorter than normal. Some women have a broad chest and/or neck and sometimes there are extra skin folds on the neck. This neck webbing can be corrected, for cosmetic reasons, with surgery. Small nails, low set ears and a low hairline may also be noticeable. In many cases only a few of the above may be present.Most girls with Turner syndrome only have a few of the characteristics associated with the condition, but short stature and infertility are nearly always present:Short statureNon-functioning ovaries leading to absence of pubertal development and infertilityExtra folds of skill on the neckPuffy hands and feetCoarctation or narrowing of the aortaFeeding problems in early childhoodBroad chest with widely spaced nipplesSmall spoon shaped nailsA low hairlineLow set earsIncreased carrying angle of the armsHearing problemsHigh blood pressureThyroid problemsDiabetesLearning difficulties (not mental retardation)Behaviour problems
What can a cervical rib lead to?
Cervical ribs are extra ribs that grow closest to the neck. They occur in between one in 200 and one in 500 people. Most people will never know they have one, and will have no symptoms. A few people will have symptoms related to thoracic outlet syndrome; this pain or numbness in the arm happens when blood vessels or nerves are compressed by the extra rib.
What is Turner stigmata?
Turner stigmata refer to the physical features associated with Turner syndrome, a genetic condition that affects females and is caused by a complete or partial absence of one of the X chromosomes. Common characteristics include short stature, webbed neck, low-set ears, and a broad chest with widely spaced nipples. Individuals with Turner syndrome may also experience various health issues, including heart defects and hormonal imbalances. Early diagnosis and intervention can help manage the symptoms and improve quality of life.
What disorder cause webbed skin in the neck?
The disorder that causes webbed skin in the neck is called branchial cleft anomalies. This condition occurs when the tissues in the neck (branchial arches) fail to develop normally during fetal development, leading to the formation of webs of skin or tissue in the neck region. Surgical intervention is usually required to correct these anomalies.
System of the body that turner's syndrome effects?
Turner syndrome (sometimes referred to Turners Syndrome)Turner syndrome -- There are two variations of the Turner's syndrome which effect females. This syndrome is caused by an abnormalities, involving the absence of all or part of one (preset with an XO karyotype), of the two normal X chromosomes. This condition entails some common developmental features which make it recognizable, as well as genetic disorders which affect a female's sexual development. Some female's with Turner syndrome (TS) may have only a few features or deformations; these can include rounded spinal thorax, webbed neck and/or a low hairline on the neck, prominent ears, lymphangiectatic edema of hands and/or the feet, cubitus valgus of the upper arm, elbow, forearm and/or hand, among other deformities; and they are shorter than average in height. This disorder causes multiple reproductive developmental issues and disorders which prevent young women from sexually maturing, causing primary amenorrhea in young women, which can leave them infertile. It can also cause congenital heart disease, causing congenital obstructive lesions of the left side of the heart in some individuals. Turner syndrome is a relatively uncommon sex-chromosome disorder which affects approximately 1 out of 2,500/3,000 births.This disorder is know by several names: Turner syndrome (Gonadal Dysgenesis) and Turner syndrome (Bonnevie-Ullrich), and the two following forms of Turner syndrome: XO syndrome(monosomy XO), females have only one X-chromosome (45 X, chromosome = karyotyped); and XX syndrome were females missing or have an incomplete X chromosome, they may have fewer or less noticeable symptoms because they still have some normal (XX) cells, (45+X, chromosome = karyotyped), the + indicating up to 90, with the additional X chromosome.Masculinized, Turner's syndrome,XY-XO mosaicism (cells with a different genetic makeup): This is a form which externally those with this form appear normal males, but they have both XY cells which are male cells, and XO cells which are Turner's syndrome female cells.This last one is not listed under Turner's syndrome or as a variation of Turner's, yet other than the physical deformities of Turner syndrome, it is a sexual deformity in that the sex glands do not develop normally.XY Gonadal Dysgenesis (Swyer syndrome)Individuals with this chromosome type are usually raised as a female and they identify as female. A person with hypogonadism is born without functional gonads, which is characterized by the failure in development of the sex glands, testicles or ovaries, (46, XY chromosome = karyotyped). It is the 46th chromosome cell that causes the disorder to be termed as Swyer Syndrome.These two disorders are associated together with many organizations which offer support groups and counseling, which offers Androgen Insensitivity Syndrome Support,www.aissg.org/21_overview.htm, groups which assists individuals with either Turner's syndrome or Swyer's syndrome. And organizations which offer more information on these disorders, such as the Society for Endocrinology,www.endocrinology.org › Links; and the Androgen Insensitivity Syndrome (AIS)/Intersex Society, www.isna.org/faq/conditions/ais.
