dc.contributor.author | ATAMER, T | |
dc.contributor.author | KIRAC, K | |
dc.contributor.author | ONAN, U | |
dc.contributor.author | SOYDINC, M | |
dc.contributor.author | SAGLAM, F | |
dc.date.accessioned | 2021-03-02T21:40:37Z | |
dc.date.available | 2021-03-02T21:40:37Z | |
dc.date.issued | 1995 | |
dc.identifier.citation | SAGLAM F., ATAMER T., ONAN U., SOYDINC M., KIRAC K., "INFANTILE GENETIC AGRANULOCYTOSIS (KOSTMANN TYPE) - A CASE-REPORT", JOURNAL OF PERIODONTOLOGY, cilt.66, sa.9, ss.808-810, 1995 | |
dc.identifier.issn | 0022-3492 | |
dc.identifier.other | av_084568c8-a2ad-4285-a795-d7b8de5cd474 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/11377 | |
dc.identifier.uri | https://doi.org/10.1902/jop.1995.66.9.808 | |
dc.description.abstract | SEVERE PERIODONTITIS IN A PATIENT WITH INFANTILE genetic agranulocytosis (Kostmann syndrome) is presented. This rare syndrome is inherited as an autosomal recessive pattern and characterized by severe neutropenia. The periodontal status and treatment of the patient is described. It is concluded that periodontal therapy including scaling, root planing, soft tissue curettage, and the use of selected antimicrobial agents can be successful in this particular syndrome. | |
dc.language.iso | eng | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Sağlık Bilimleri | |
dc.subject | DİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP | |
dc.subject | Klinik Tıp | |
dc.subject | Tıp | |
dc.subject | Diş Hekimliği | |
dc.title | INFANTILE GENETIC AGRANULOCYTOSIS (KOSTMANN TYPE) - A CASE-REPORT | |
dc.type | Makale | |
dc.relation.journal | JOURNAL OF PERIODONTOLOGY | |
dc.contributor.department | , , | |
dc.identifier.volume | 66 | |
dc.identifier.issue | 9 | |
dc.identifier.startpage | 808 | |
dc.identifier.endpage | 810 | |
dc.contributor.firstauthorID | 116588 | |