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Turner's syndrome

American  

noun

Pathology.
  1. an abnormal congenital condition resulting from a defect on or absence of the second sex chromosome, characterized by retarded growth of the gonads.


Etymology

Origin of Turner's syndrome

Named after Henry Hubert Turner (1892–1970), U.S endocrinologist, who described it in 1938

Example Sentences

Examples are provided to illustrate real-world usage of words in context. Any opinions expressed do not reflect the views of Dictionary.com.

A female with Turner’s syndrome usually inherits only one X chromosome.

From Textbooks • Jan. 1, 2018

Nondisjunction of the X chromosomes can lead to a disorder known as Turner’s syndrome.

From Textbooks • Jan. 1, 2018

In about 1 in 5,000 cases, a fetus may have only a single chromosome—an X—a condition known as Turner’s syndrome.

From Scientific American • Jul. 27, 2013

Girls with Turner's syndrome have only a single complete X, and it can come from either Mom or Dad; modern genetic tests can reveal which.

From Time Magazine Archive

Girls who suffer from the rare genetic disorder known as Turner's syndrome are a little shorter than average, have a thicker neck and usually can't have children.

From Time Magazine Archive