What is the history behind Turner syndrome?
The history of Turner syndrome began in 1938, when Henry Turner described 7 patients between the ages of 15 and 23, who were referred to him for dwarfism and lack of sexual development. He treated them with pituitary extracts, but they were ineffective.
When was Turner syndrome first diagnosed?
Turner syndrome was first discovered in 1938 by Dr.
How did Turner syndrome get its name?
Turner syndrome is named for Henry Turner who, in 1938, was one of the first doctors to report on the disorder in the medical literature. Turner syndrome is one of the most common chromosomal disorders and likely the most common genetic disorder of females.
Can Turner syndrome be cured?
There’s no cure for Turner syndrome but many of the associated symptoms can be treated.
Who was the first person to discover Turner syndrome?
Turner Syndrome was first described in 1938 by Dr. Henry Turner, but chromosomal abnormalities were not discovered until 1960. Dr Turner was an endocrinologist from Oklahoma City who discovered Turner Syndrome when a group of women he was treating for dwarfism didn’t respond to treatments.
Who is the founder of mosaic Turner syndrome?
This syndrome is also referred to as Mosaic Turner Syndrome and Ullrich-Turner Syndrome and is a genetic condition that affects the sexual development in females. Turner Syndrome was discovered in 1938 by Dr. Henry. This syndrome affects approximately one in two thousand five hundred female births everywhere.
How many women are affected by Turner syndrome?
Turner Syndrome was discovered in 1938 by Dr. Henry. This syndrome affects approximately one in two thousand five hundred female births everywhere. Usually if a woman is carrying a female fetus with this syndrome the pregnancy does not survive.
How is Turner syndrome ( TS ) treated in the US?
TS is not directly treated by a doctor, but the individual health concerns that arise for each girl or woman with TS should be monitored and treated by an appropriate specialist. Treatment should be individualized and physicians, families, and patients should decide on treatment options together.
What is the cure for Turner syndrome?
There is no cure for Turner syndrome, but therapies have been developed that can improve physical development. With proper medical care, females with Turner syndrome should be able to lead full, productive lives. The primary therapies for affected individuals are growth hormone therapy and estrogen therapy.
What causes Turner syndrome?
Turner syndrome (TS) is a genetic disorder caused by the partial or complete absence of one X chromosome. This is called monosomy and is typically caused by chromosomal nondisjunction.
What is the inheritance of Turner syndrome?
Turner syndrome is not usually inherited from a person’s parents. No environmental risks are known, and the mother’s age does not play a role. Turner syndrome is due to a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes,…
How common is Turner’s syndrome?
Turner syndrome occurs in about 1 in 2,500 female births worldwide, but is much more common among pregnancies that do not survive to term (miscarriages and stillbirths). Prenatal testing has probably decreased the number of diagnosed cases of Turner syndrome.