FRAGILE X SYNDROME: CLINICAL & CYTOLOGICAL STUDY IN NORTH KARNATAKA

DR R.S.BULAGOUDADR G.S.KADAKOL, DR M M PATIL, DR S.V.PATIL,  DR BHEEMSHETTY S. PATIL

dc.contributor.author	DR R.S.BULAGOUDADR G.S.KADAKOL, DR M M PATIL, DR S.V.PATIL, DR BHEEMSHETTY S. PATIL
dc.date.accessioned	2019-11-06T07:20:20Z
dc.date.available	2019-11-06T07:20:20Z
dc.date.issued	2017-04
dc.identifier.uri	http://hdl.handle.net/123456789/1140
dc.description.abstract	Fragile-X syndrome (FXS) is the most common inherited form of mental disorder. The clinical features of FXS include moderate to severe mental retardation, dysmorphic facial features. One such case was seen & admitted in our hospital with similar clinical symptoms. We examined both clinical and cytological analysis. After examining all these we found child with Fragile X Syndrome. We suggest that molecular analysis of Fragile X Syndrome related to FMR1gene will help to know the novel mutation in this population, which will be helpful for early diagnosis of Fragile-X syndrome and type of genetic disorder.	en_US
dc.language.iso	en	en_US
dc.publisher	BLDE(Deemed to be University)	en_US
dc.subject	Fragile X Syndrome (FXS), Mental retardation, Cytogenetic Analysis, Clinical case Fragile X Syndrome.	en_US
dc.title	FRAGILE X SYNDROME: CLINICAL & CYTOLOGICAL STUDY IN NORTH KARNATAKA	en_US
dc.type	Article	en_US