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dc.contributor.authorKaraca, Meryem
dc.contributor.authorCakar, Nafiye Emel
dc.date.accessioned2021-03-02T22:21:19Z
dc.date.available2021-03-02T22:21:19Z
dc.date.issued2020
dc.identifier.citationCakar N. E. , Karaca M., "EVALUATION OF HEMATOLOGIC FINDINGS IN MUCOPOLYSACCHARIDOSIS CASES", ACTA MEDICA MEDITERRANEA, cilt.36, sa.2, ss.797-800, 2020
dc.identifier.issn0393-6384
dc.identifier.otherav_0c2fc763-0b12-44f0-89c4-7ddec432afbf
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/13840
dc.identifier.urihttps://doi.org/10.19193/0393-6384_2020_2_123
dc.description.abstractIntroduction: Mucopolysaccharidosis (MPS) are lysosomal storage diseases characterized by chronic, progressive and multiple system involvement due to impaired glycosaminoglycans destruction. There are 7 types of MPS as type I, II, III, IV, VI, VII and IX. There is wide clinical heterogeneity, coarse face, cardiac involvement, deafness, bone dysplasia, corneal clouding, learning difficulties.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectTemel Tıp Bilimleri
dc.titleEVALUATION OF HEMATOLOGIC FINDINGS IN MUCOPOLYSACCHARIDOSIS CASES
dc.typeMakale
dc.relation.journalACTA MEDICA MEDITERRANEA
dc.contributor.departmentOkmeydani Training & Educ Hosp , ,
dc.identifier.volume36
dc.identifier.issue2
dc.identifier.startpage797
dc.identifier.endpage800
dc.contributor.firstauthorID1044098


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