Clinical manifestations of tuberous sclerosis complex

dc.contributor.authorAtay A.E.
dc.contributor.authorAkbas H.
dc.contributor.authorSakar N.
dc.contributor.authorPasa S.
dc.contributor.authorAri S.
dc.contributor.authorEkin N.
dc.date.accessioned2024-04-24T18:45:47Z
dc.date.available2024-04-24T18:45:47Z
dc.date.issued2013
dc.departmentDicle Üniversitesien_US
dc.description.abstractTuberous sclerosis complex (TSC) is an autosomal dominant syndrome or in sporadic form characterized by hamartamatous lesions in multiple organs. It affects several sites such as skin, kidney, lung, heart, central nervous system and liver in diferent stages of disease. TSC is caused by mutations on either chromosome 9 (9q34, the TSC1 gene) or chromosome 16 (16p13, TSC2 gene). TSC1 and TSC2 genes encode proteins called tuberin and hamartin; respectively. Although the pathogenetic mechanism is exactly unknown, a possible mechanism is a GTPase-activating protein against Rheb (Ras homolog enriched in brain), which regulates mTOR (mammalian target of rapamycin) signaling. The mammalian target of rapamycin (mTOR), is a serine-threonine kinase that increases cell proliferation and growth. We aimed to review the clinical manifestations and their predictive role on the course of disease.en_US
dc.identifier.endpage57en_US
dc.identifier.issn1301-0883
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-84879749160
dc.identifier.scopusqualityQ4
dc.identifier.startpage52en_US
dc.identifier.urihttps://hdl.handle.net/11468/24881
dc.identifier.volume18en_US
dc.indekslendigikaynakScopus
dc.language.isoenen_US
dc.publisherYuzuncu Yil Universitesi Tip Fakultesien_US
dc.relation.ispartofEastern Journal of Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAutosomal Dominanten_US
dc.subjectTuberous Sclerosisen_US
dc.titleClinical manifestations of tuberous sclerosis complexen_US
dc.titleClinical manifestations of tuberous sclerosis complex
dc.typeReview Articleen_US

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