Turner syndrome
Jump to navigation
Jump to search
English[edit]
Etymology[edit]
Named after Henry Turner who first described the condition in 1938.
Noun[edit]
- (medicine, medical genetics) A particular genetic condition, caused by partially or completely missing an X chromosome (monosomy), that leads to sterility and other issues.
Translations[edit]
disease
|
Further reading[edit]
- Turner syndrome on Wikipedia.Wikipedia
- “Turner syndrome”, in OneLook Dictionary Search.