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CLINICAL AND CYTOLOGICAL STUDY ON TURNER SYNDROME

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dc.contributor.author RUDRAGOUDA S BULAGOUDA GAVISHIDDAPPA HADIMANIGURUSHANTAPPA S KADAKOL SHANKAR V PATIL
dc.date.accessioned 2019-11-06T07:49:58Z
dc.date.available 2019-11-06T07:49:58Z
dc.date.issued 2017-01
dc.identifier.uri http://hdl.handle.net/123456789/1141
dc.description.abstract Turner syndrome (TS) is a common chromosomal disorder. TS also known as Ulrich-TS. Gonadal dysgenesis, 45X is a condition in which there is partly or completely missing X chromosome in a female. The main clinical features of TS are swollen hands and feet, wide, and webbed neck. A combination of the following symptoms may be seen in older females: Absent or incomplete development of puberty (sparse pubic hair and small breasts), broad and shield like chest, drooping eyelids. TS frequently seen in young infants. Our case is a 10-year-old girl with TS-specific clinical hallmarks, with the symptoms of en_US
dc.language.iso en en_US
dc.publisher BLDE(Deemed to be University) en_US
dc.subject TURNER SYNDROME en_US
dc.title CLINICAL AND CYTOLOGICAL STUDY ON TURNER SYNDROME en_US
dc.type Article en_US


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