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dc.contributor.authorEkmektzoglou, Konstantinos A.
dc.contributor.authorDemestiha, Theano D.
dc.contributor.authorTroupis, Georgios T.
dc.contributor.authorXanthos, Theodoros
dc.creatorEkmektzoglou, Konstantinos A.
dc.date.accessioned2019-01-31T07:32:24Z
dc.date.available2019-01-31T07:32:24Z
dc.date.issued2012-04-01
dc.identifierSCOPUS_ID:84858163470
dc.identifier.issn15513815
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84858163470&origin=inward
dc.identifier.urihttps://repo.euc.ac.cy/handle/123456789/1656
dc.description.abstractOvergrowth syndromes, although rare, are diagnosed more frequently lately. Major progress, such as the identification of genetic causes, has recently enhanced the delineation of the characteristic and noncharacteristic manifestations, phenotype-genotype correlations and knowledge of the underlying pathophysiologic mechanisms. This review provides a summary of the most important overgrowth syndromes aiming to familiarize the treating physician with the cardinal clinical features involved in these syndromes that encompass overgrowth, but also have a variety of other clinical manifestations (neurologic, musculoskeletal, skin, and accompanying tumors).
dc.relation.ispartofFetal and Pediatric Pathology
dc.titleCommonest overgrowth syndromes
elsevier.identifier.doi10.3109/15513815.2011.650293
elsevier.identifier.eid2-s2.0-84858163470
elsevier.identifier.scopusidSCOPUS_ID:84858163470
elsevier.volume31
elsevier.issue.identifier2
elsevier.coverdate2012-04-01
elsevier.coverdisplaydateApril 2012
elsevier.openaccess0
elsevier.openaccessflagfalse
elsevier.aggregationtypeJournal


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