Turner Syndrome
Turner Syndrome is a chromosomal disorder caused by a complete or partial absence of the second X chromosome in females. It is a genetic condition that affects females only, and affects approximately 1 out of every 2,500 female live births. Common physical features of those with the disorder include a webbed neck, low-set ears, extra folds of skin on the neck, swollen hands and feet, and a short stature. Intellectual and developmental delays, heart abnormalities and infertility may also occur. With appropriate medical care, individuals with Turner Syndrome can lead normal, healthy lives. Early diagnosis and management of health issues associated with the disorder is essential for individuals to lead productive, healthy lives. Treatment usually includes growth hormone therapy, fertility treatments, and gonadotropin-releasing hormone agonists to induce puberty.
← Journal of Chromosomes