Congenital Insensitivity to Pain with Anhidrosis Syndrome: A Case Report

Basit Öğe Kaydı
dc.contributor.authorTuran, Hakan
dc.contributor.authorBesir, Fahri Halit
dc.contributor.authorUslu, Esma
dc.contributor.authorBasar, Feyza
dc.contributor.authorGun, Emrah
dc.contributor.authorGecer, Yavuz
dc.date.accessioned2024-09-25T19:59:46Z
dc.date.available2024-09-25T19:59:46Z
dc.date.issued2014
dc.departmentAbant İzzet Baysal Üniversitesien_US
dc.description.abstractCongenital Insensitivity to Pain with Anhidrosis syndrome is a rare, autosomal recessively inherited syndrome caused by neurotrophic tyrosine receptor kinase 1 gene mutation. The basic findings of the syndrome are absence of pain sense, anhidrosis, and self-destructive behaviors. Herein, we describe a 4-year-old boy presented with xerosis, anhidrosis, and traumatic lesions on the hands and diagnosed as Congenital Insensitivity to Pain with Anhidrosis syndrome. On the occasion of this case, we aimed to review general and dermatological characteristics of this rare syndrome.en_US
dc.identifier.doi10.4274/tdd.1528
dc.identifier.endpage44en_US
dc.identifier.issn1307-7635
dc.identifier.issn1308-5255
dc.identifier.issue1en_US
dc.identifier.startpage42en_US
dc.identifier.urihttps://doi.org/10.4274/tdd.1528
dc.identifier.urihttps://hdl.handle.net/20.500.12491/13894
dc.identifier.volume8en_US
dc.identifier.wosWOS:000420904400009en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isotren_US
dc.publisherGalenos Yayinciliken_US
dc.relation.ispartofTurk Dermatoloji Dergisi-Turkish Journal of Dermatologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.snmzYK_20240925en_US
dc.subjectPainen_US
dc.subjectanhidrosisen_US
dc.subjectcongenitalen_US
dc.subjectneuropathyen_US
dc.titleCongenital Insensitivity to Pain with Anhidrosis Syndrome: A Case Reporten_US
dc.typeArticleen_US

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