Gaucher Disease for Hematologists

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dc.contributor.authorÖzdemir, G.N.
dc.contributor.authorGündüz, E.
dc.date.accessioned2024-05-19T14:33:19Z
dc.date.available2024-05-19T14:33:19Z
dc.date.issued2022
dc.departmentİstinye Üniversitesien_US
dc.description.abstractGaucher disease (GD) is a rare hereditary lysosomal storage disease that arises due to deficiency of glucocerebrosidase. Early diagnosis is very important for starting proper treatment and preventing complications. Splenomegaly, anemia, and thrombocytopenia are the most common findings in GD and so most patients are initially referred to hematologists. The Turkish Society of Hematology established its Rare Hematological Diseases Subcommittee in 2015. One of the main topics of this subcommittee was to increase and improve awareness and education of rare diseases among hematologists in Turkey. This review presents GD with an overview of its clinical features, pathophysiology, and treatment options for hematologists. © 2022 by Turkish Society of Hematology.en_US
dc.description.sponsorshipreceived no financial support.en_US
dc.identifier.doi10.4274/tjh.galenos.2022.2021.0683
dc.identifier.endpage139en_US
dc.identifier.issn1300-7777
dc.identifier.issue2en_US
dc.identifier.pmid35439918en_US
dc.identifier.scopus2-s2.0-85131225324en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage136en_US
dc.identifier.urihttps://doi.org/10.4274/tjh.galenos.2022.2021.0683
dc.identifier.urihttps://hdl.handle.net/20.500.12713/4184
dc.identifier.volume39en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherTurkish Society of Hematologyen_US
dc.relation.ispartofTurkish Journal of Hematologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.snmz20240519_kaen_US
dc.subjectAnemiaen_US
dc.subjectGaucher Diseaseen_US
dc.subjectSplenomegalyen_US
dc.subjectThrombocytopeniaen_US
dc.titleGaucher Disease for Hematologistsen_US
dc.typeArticleen_US

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