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http://20.193.157.4:9595/xmlui/handle/123456789/1141Full metadata record
| DC Field | Value | Language |
|---|---|---|
| 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 |
| Appears in Collections: | Faculty of Anatomy | |
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