a chromosomal disorder, specific to females, marked by the absence of all or a part of one of the two X (female) chromosomes. The effects include
gonadal dysgenesis (underdevelopment or absence of primary and secondary
sex characteristics), infertility, and various other abnormalities (e.g., short stature, lack of menstruation). Although the disorder is genetic, it is not inherited, occurring instead as a random event during cell division in early fetal development. See also
Noonan syndrome. [reported in 1938 by Henry H. Turner (1892–1970), U.S. endocrinologist]