Turner Syndrome

Turner syndrome

Click here to download instantly!

16p11.2 deletion syndrome: MedlinePlus Genetics

So you just found out your daughter has Turner Syndrome. This post may contain affiliate links.

For more information, you can read my disclosure statement here. What Is Turner Syndrome Turner Syndrome, also known as gonadal dysgenesis, is a rare chromosomal condition that only affects females.

It was first described by Dr. Henry Turner in Although Turner Syndrome is rare, affecting only 1 out of every 2, births, it the most common sex chromosomal disorders in females. Turner Syndrome, or TS, is characterized by a partial or completely missing X chromosome, and this Turner syndrome TS into two main types: Monosomy - complete loss of the second X chromosome Mosaic - partial loss of the second X chromosome As a reminder, most people have Turner syndrome chromosomes, 23 of which are inherited from the mother, and 23 are inherited from the father.

Turner syndrome a male, the mother contributes an X chromosome and the father contributes a Y chromosome, creating an XY pair. In a female, the mother contributes an X chromosome and the father also contributes an X chromosome, resulting in an XX pair. As I mentioned earlier, TS only occurs in females.

This is because males only have Turner syndrome X chromosome and if that X chromosome is partially or completely missing, life is not viable. In contrast, females have two X chromosomes, which means that damage to one X chromosome still leaves another complete X chromosome, making life viable. The exact cause of TS is thought to be random.]

Turner syndrome - consider

Henry Turner first described Turner Syndrome. Turner Syndrome a genetic disease that only affects girls, in fact, it is one of the most common sexual development disorders Radtke et al. It is caused by an abnormal sex chromosome, either an abnormal X chromosome or a missing X chromosome. The sex chromosome contributed by the father to the child determines the sex of the child because the mother always contributes an X chromosome whereas the father can contribute either an X chromosome Turner syndrome Essay Words 5 Pages including: hereditary factors short parents , diseases affecting the kidneys; heart, lungs or intestines; hormone imbalances; severe stress or emotional deprivation; infections in the womb before birth; bone diseases; and genetic or chromosomal abnormalities. A German doctor named Ullrich published his article in American doctor Henry Turner recognized a pattern of short stature and incomplete Turner Syndrome Words 4 Pages Introduction Named after Henry Turner, who in was one the first doctors to report his discovery in the medical literature on this disorder, Turner Syndrome TS also known as monosomy X. Turner Syndrome is caused by the complete or partial loss of one of the X chromosomes resulting in 45X chromosomes. Turner syndrome.

This magnificent: Turner syndrome

Comparing Odysseuss Strengths And Weaknesses	1000
NARCISSISM ANALYSIS	739
Turner syndrome	23 hours ago · Dysgenesis Gonadal Dysgenesis, also known as turner syndrome, is a rare medical disorder that affects 1 in every 2, 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. 2 days ago · Turner Syndrome is a chromosomal condition that occurs when one of the X chromosomes is missing or partially missing. Turner Syndrome is most commonly diagnosed during pregnancy or early infancy/childhood, but in rare cases can be diagnosed in adolescence. It only affects girls because. 2 days ago · Turner syndrome is a chromosomal condition related to the X chromosome that alters development in females, though it is not usually inherited in families Donate Turner syndrome can affect one person very differently from how it affects another person.