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turners syndrome

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Turner's syndrome

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

Origin:
named after Henry Hubert Turner (1892–1970), U.S endocrinologist, who described it in 1938
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Based on the Random House Dictionary, © Random House, Inc. 2009.
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Medical Dictionary

Main Entry: Tur·ner's syndrome
Pronunciation: 't&r-n&rz-
Variant: or Tur·ner syndrome /-n&r-/
Function: noun
: a genetically determined condition that is typically associated with the presence of only one complete X chromosome and no Y chromosome and with characteristics including a female phenotype,underdeveloped and usually infertile ovaries, absence of menstrual onset, short stature, excess skin about the neck, cubitus valgus, aortic coarctation, and a low hairline on the back of the neck
Turner, Henry Hubert (1892–1970), American endocrinologist. Turner practiced internal medicine privately and served as a consulting endocrinologist and chief of ametabolic clinic at a university hospital in Oklahoma. He described Turner's syndrome in 1938.
Merriam-Webster's Medical Dictionary, © 2002 Merriam-Webster, Inc.
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Medical Dictionary

Turner's syndrome Tur·ner's syndrome (tûr'nərz)
n.
A congenital condition of females associated with a defect or an absence of an X-chromosome, characterized by short stature, webbed neck, outward-turning elbows, shield-shaped chest, sexual underdevelopment, and amenorrhea. Also called XO syndrome.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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