What is the inheritance pattern of Wilson-Turner syndrome?

Wilson-Turner syndrome, also known as Turner syndrome, is primarily associated with the absence of all or part of a second sex chromosome in females, which largely affects sexual development and physical characteristics. The inheritance pattern of this condition is not strictly X-linked in the classical sense; rather, it arises due to a chromosomal abnormality.

When discussing Wilson-Turner syndrome, it manifests from a nondisjunction during meiosis, leading to the total or partial loss of an X chromosome. This nondisjunction event is random and does not follow typical Mendelian inheritance patterns such as autosomal dominant or autosomal recessive inheritance.

Thus, recognizing that Turner syndrome arises from chromosomal-level changes and is fundamentally related to sex chromosome anomalies aids in understanding why it relates to the X chromosome and why categorizing it simply under X-linked inheritance can sometimes lead to confusion. However, since the option of "X-linked" is the closest available choice provided, it can be selected, while keeping in mind the nature of chromosomal abnormalities involved in this syndrome.