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dc.contributor.authorIlguy, D
dc.contributor.authorOzcan, I
dc.contributor.authorSirin, S
dc.contributor.authorErdem, TL
dc.date.accessioned2021-03-03T15:27:20Z
dc.date.available2021-03-03T15:27:20Z
dc.date.issued2000
dc.identifier.citationErdem T., Ozcan I., Ilguy D., Sirin S., "Hereditary sensory and autonomic neuropathy: review and a case report with dental implications", JOURNAL OF ORAL REHABILITATION, cilt.27, sa.2, ss.179-182, 2000
dc.identifier.issn0305-182X
dc.identifier.othervv_1032021
dc.identifier.otherav_3f0a71a0-aa2c-486b-a0cc-6d1a479c6fd4
dc.identifier.urihttp://hdl.handle.net/20.500.12627/46204
dc.identifier.urihttps://doi.org/10.1046/j.1365-2842.2000.00474.x
dc.description.abstractHereditary sensory and autonomic neuropathy (HSAN) is a rare syndrome which is seen in early childhood. Five different types are described. Absence of pain and self-mutilation are characteristic findings of this syndrome. Teeth in the oral cavity can cause damage to the oral tissues and tongue. When it is diagnosed, there should be co-operation between dentist and neurologist. Using an oral shield prevents the biting and, thus, traumatization of the tissues can be prevented. A case report which is diagnosed as HSAN type 4 is presented and information submitted about its treatment.
dc.language.isoeng
dc.subjectTıp
dc.subjectDiş Hekimliği
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.titleHereditary sensory and autonomic neuropathy: review and a case report with dental implications
dc.typeMakale
dc.relation.journalJOURNAL OF ORAL REHABILITATION
dc.contributor.department, ,
dc.identifier.volume27
dc.identifier.issue2
dc.identifier.startpage179
dc.identifier.endpage182
dc.contributor.firstauthorID125103


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