What is Turners Syndrome?
Turner’s Syndrome is a genetic disorder that can cause premature ovarian failure, in which a woman is born without the second X chromosome or without part of it. Causes deficient ovarian development — and often primary amenorrhea. It is a genetic disorder in girls that occurs in approximately 1 in 2,500 live births and results in short stature and failure to develop secondary sexual characteristics. Human growth hormone is effective in promoting growth and improving final height in girls with this condition. Zomacton, Human Growth Factor, has now been approved for Turners Syndrome. Read more about Zomacton.
Turner’s syndrome is a condition that affects approximately one in 200 females. The condition does not affect men. Turner’s syndrome occurs when both of the X chromosomes normally found in women are missing. Chromosomes are the deoxyribonucleic acid (DNA) strands found in every cell in the body. In Turner’s syndrome, the X chromosomes may be completely missing or only partially present. If the X chromosomes are completely missing, the condition is medically designated as Classic Turner’s Syndrome. The most common symptoms of Classic Turner’s syndrome include physical shortness and infertility due to non-development of the ovaries. The symptoms of Turner’s syndrome vary from female to female. They can include a very low hairline, a webbed neck, a wide chest with nipples that are spaced far apart, and low set ears. Other symptoms may include swollen looking hands and feet and the appearance of a variety of small birthmarks. Women who suffer from Turner’s syndrome may also develop a numbe
