Structured Summary
Abstract
A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant.
MeSH Record
Classification
Related Concepts
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MeSH Record
See Also
MeSH Record
Synonyms
13 entry terms
- Turner's Syndrome
- Ullrich-Turner Syndrome
- Syndrome, Ullrich-Turner
- Turners Syndrome
- Ullrich Turner Syndrome
- Bonnevie-Ullrich Syndrome
- Gonadal Dysgenesis, 45,X
- Gonadal Dysgenesis, XO
- Monosomy X
- Status Bonnevie-Ullrich
- Bonnevie Ullrich Syndrome
- Status Bonnevie Ullrich
- XO Gonadal Dysgenesis
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
in females; TURNER SYNDROME, MALE see NOONAN SYNDROME is also available
MeSH Record
History Note
2002(1963); for BONNEVIE-ULLRICH SYNDROME use SEX CHROMOSOME ABNORMALITIES 1963-2001
MeSH Hierarchy
Tree Numbers
- C12.050.351.875w.253w.309w.872w
- C12.050.351.875w.253w.795.750w
- C12.200.706w.316w.309w.872w
- C12.200.706w.316w.795.750w
- C12.800w.316w.309w.872w
- C12.800w.316w.795.750w
- C14w.240.400w.980w
- C14w.280w.400w.980w
- C16w.131w.240.400w.970w
- C16w.131w.260w.830w.835.750w
- C16w.131w.939w.316w.309w.872w
- C16w.131w.939w.316w.795.750w
- C16w.320w.180w.830w.835.750w
- C19w.391.119w.309w.872w
- C19w.391.119w.795.750w
MeSH Record
NLM Classification
WP 101
AMA Style
References
- National Library of Medicine. Turner Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D014424. http://id.nlm.nih.gov/mesh/2026/D014424
- Turner Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Turner_syndrome
- Turner Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q202849