Niemann-pick type b disease diagnosed in the adulthood

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dc.contributor.authorDemircioğlu, Sinan
dc.contributor.authorKorkmaz, Celalettin
dc.contributor.authorÇizmecioğlu, Hilal Akay
dc.contributor.authorPoyraz, Necdet
dc.date.accessioned2020-03-26T19:44:50Z
dc.date.available2020-03-26T19:44:50Z
dc.date.issued2018
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractNiemann-Pick disease (NPD) type B is an autosomal recessive liposomal storage disorder. NPD type B can present later inlife with predominantly visceral symptoms, and has a more favorable prognosis. The natural history of NPD -B is one ofprogressive hypersplenism and gradual deterioration of pulmonary function. In this paper, we presented NPD type Bpatient who were diagnosed at 41 years old while being followed for years with the diagnosis of interstitial lung disease.en_US
dc.identifier.citationDemircioğlu S., Korkmaz C., Çizmecioğlu H. A., Poyraz N. (2018). Niemann-pick type b disease diagnosed in the adulthood. Eastern Journal of Medicine, 23(4), 322-324.
dc.identifier.doi10.5505/ejm.2018.19484en_US
dc.identifier.endpage324en_US
dc.identifier.issn1301-0883en_US
dc.identifier.issn1339-3886en_US
dc.identifier.issue4en_US
dc.identifier.startpage322en_US
dc.identifier.urihttps://dx.doi.org/10.5505/ejm.2018.19484
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TXpJMU9USTRPQT09
dc.identifier.urihttps://hdl.handle.net/20.500.12395/35938
dc.identifier.volume23en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofEastern Journal of Medicineen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectDiş Hekimliğien_US
dc.subjectFarmakoloji ve Eczacılıken_US
dc.subjectToksikolojien_US
dc.titleNiemann-pick type b disease diagnosed in the adulthooden_US
dc.typeArticleen_US

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