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Dyskeratosis congenita associated with Hodgkin's disease

dc.contributor.authorKAVAK, Ayşe
dc.contributor.authorBaykal, Can
dc.contributor.authorBuyukbabani, Nesimi
dc.date.accessioned2021-03-03T20:14:05Z
dc.date.available2021-03-03T20:14:05Z
dc.date.issued1998
dc.identifier.citationBaykal C., Buyukbabani N., KAVAK A., "Dyskeratosis congenita associated with Hodgkin's disease", EUROPEAN JOURNAL OF DERMATOLOGY, cilt.8, sa.6, ss.385-387, 1998
dc.identifier.issn1167-1122
dc.identifier.othervv_1032021
dc.identifier.otherav_58da2655-a414-4db1-9eca-bca9fc14c15a
dc.identifier.urihttp://hdl.handle.net/20.500.12627/62534
dc.description.abstractDyskeratosis congenita is a rare, hereditary, multisystem disorder characterized by mucocutaneous changes, pancytopenia and increased incidence of malignancy. Different types of neoplasia have been reported in association with dyskeratosis congenita. We present a second case associated with Hodgkin's disease. Delayed appearance of dermatological signs and association with chronic hepatitis B are other unusual features of this case.
dc.language.isoeng
dc.subjectDERMATOLOJİ
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectDermatoloji
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.titleDyskeratosis congenita associated with Hodgkin's disease
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF DERMATOLOGY
dc.contributor.department, ,
dc.identifier.volume8
dc.identifier.issue6
dc.identifier.startpage385
dc.identifier.endpage387
dc.contributor.firstauthorID23224


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