Partial Merosin Deficiency and Precocious Puberty

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dc.contributor.authorEklioglu, Beray Selver
dc.contributor.authorAkyurek, Nesibe
dc.contributor.authorYuca, Sevil Ari
dc.contributor.authorAtabek, Mehmet Emre
dc.date.accessioned2024-02-23T14:31:58Z
dc.date.available2024-02-23T14:31:58Z
dc.date.issued2015
dc.departmentNEÜen_US
dc.description.abstractThe congenital muscular dystrophies (CMD) are autosomal-recessive disorders. Classical congenital muscular dystrophy is grouped as merosin-positive and merosin-negative (MN-CMD). Precocious puberty in girls has been defined by Marshal and Tanner in 1969. In most of the cases, precocious puberty is idiopathic and is related to premature release of gonadotrophins. So far, the association between merosin deficiency and precocious puberty has not been identified. We report a case of a child with precocious puberty who was diagnosed with merosin deficiency in infancy.en_US
dc.identifier.doi10.15197/sabad.1.12.18
dc.identifier.endpage92en_US
dc.identifier.issn1304-3889
dc.identifier.issn1304-3897
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-84926016204en_US
dc.identifier.startpage90en_US
dc.identifier.urihttps://doi.org/10.15197/sabad.1.12.18
dc.identifier.urihttps://hdl.handle.net/20.500.12452/15433
dc.identifier.volume12en_US
dc.identifier.wosWOS:000367540700018en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherModestum Ltden_US
dc.relation.ispartofEuropean Journal Of General Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectPrecocious Pubertyen_US
dc.subjectMerosin Deficiencyen_US
dc.subjectChilden_US
dc.titlePartial Merosin Deficiency and Precocious Pubertyen_US
dc.typeArticleen_US

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