2020
Overview
Turner Syndrome is a genetic disorder affecting females from birth due to the absence or abnormality of one of the X chromosomes. The deficiency results in underdeveloped ovaries and infertility in most cases, and it can also cause various medical and developmental problems. One of the most common symptoms of Turner Syndrome is short stature, as a lack of the hormone typically produced by the ovaries (estrogen) during puberty can prevent growth spurts. Individuals with Turner Syndrome may also have a webbed neck and puffy hands and feet, and they may be prone to certain health issues such as heart or kidney abnormalities, high blood pressure, and osteoporosis. Reproductive health complications associated with Turner Syndrome typically require ongoing medical management, such as hormone replacement therapy to facilitate normal puberty development and the potential for fertility treatments later in life. Aside from medical considerations, many individuals with Turner Syndrome also face social and emotional challenges related to the disorder. For example, low self-esteem, difficulty forming friendships, and difficulty with social cues are common among girls with Turner Syndrome. In summary, Turner Syndrome is a complex genetic disorder that can impact reproductive and overall health, as well as social and emotional well-being. It is essential to raise awareness of and provide support for those affected by Turner Syndrome to ensure they receive appropriate care and understanding.
Research published in this journal
1 peer-reviewed article, ranked by relevance. Each links to its DOI.