What is Turner syndrome explain its symptoms?
Features of Turner syndrome may include a short neck with a webbed appearance, low hairline at the back of the neck, low-set ears, hands and feet that are swollen or puffy at birth, and soft nails that turn upward. Stature. Girls with Turner syndrome grow more slowly than other children.
What are three symptoms of Turner syndrome?
Signs of Turner syndrome at birth or during infancy may include:
- Wide or weblike neck.
- Low-set ears.
- Broad chest with widely spaced nipples.
- High, narrow roof of the mouth (palate)
- Arms that turn outward at the elbows.
- Fingernails and toenails that are narrow and turned upward.
What is the main cause of Turner syndrome?
Turner syndrome is caused by partial or complete loss (monosomy) of the second sex chromosome. Chromosomes are found in the nucleus of all body cells. They carry the genetic characteristics of each individual and they come in pairs.
What is Turner syndrome known as?
Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic condition in which a female is partly or completely missing an X chromosome. Signs and symptoms vary among those affected.
What is Turner syndrome Class 12?
Turner syndrome is a female-specific genetic condition caused by a partial or total deletion of one of the X chromosomes. Turner syndrome is also known as monosomy of the X chromosome.
How does Turner syndrome occur?
Turner syndrome occurs when part or all of an X chromosome is missing from most or all of the cells in a girl’s body. A girl normally receives one X chromosome from each parent. The error that leads to the missing chromosome appears to happen during the formation of the egg or sperm.
How many types of Turner syndrome are there?
There are 2 types of Turner syndrome: monosomy X TS and mosaic TS. About half of all girls with Turner syndrome have a monosomy disorder. Monosomy means that a person is missing one chromosome in the pair. Instead of 46 chromosomes, the person has only 45 chromosomes.
What famous person has Turner syndrome?
Actress Linda Hunt and gymnast Misty Marlowe, Scottish actress Janette Cranky have Turner’s syndrome.
How do you diagnose Turner syndrome?
A genetic test called a karyotype analysis can confirm a Turner syndrome diagnosis. This test requires a blood draw. It can determine whether one of the X chromosomes is fully or partially missing. A complete heart evaluation is also part of diagnosis.
What race is Turner syndrome most common in?
During 2012-2016 (average) in North Carolina, Turner syndrome was highest for American Indian infants (5.1 in 10,000 live female births), followed by whites (2.3 in 10,000 live female births), Hispanics (1.8 in 10,000 live female births), blacks (1.1 in 10,000 live female births) and Asians (0.8 in 10,000 live female …
Why can’t males have Turner syndrome?
Turner syndrome is caused by a female having one normal X chromosome in each of her cells , while the other sex chromosome is either missing or structurally abnormal. Females without Turner syndrome have 2 full X chromosome in all of their cells, and males have one X chromosome and one Y chromosome .