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dc.contributor.authorImren, Yunus
dc.contributor.authorŞEN, Cengiz
dc.contributor.authorUruc, Vedat
dc.contributor.authorKucukdurmaz, Fatih
dc.date.accessioned2022-02-18T11:24:40Z
dc.date.available2022-02-18T11:24:40Z
dc.date.issued2015
dc.identifier.citationKucukdurmaz F., Imren Y., Uruc V., ŞEN C., "Congenital Insensitivity to Pain with Anhidrosis (CIPA) Manifested with Chronic Osteomyelitis; A Case Report", JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE, cilt.6, sa.2, ss.230-232, 2015
dc.identifier.othervv_1032021
dc.identifier.otherav_f4773ca1-40dc-4813-9684-71bb22586089
dc.identifier.urihttp://hdl.handle.net/20.500.12627/181131
dc.identifier.urihttps://doi.org/10.4328/jcam.912
dc.description.abstractChronic osteomyelitis is a very rare entity among children. Also congenital insen-sitivity to pain with anhidrosis (CIPA) is a very rare autosomal-recessive disease of the nervous system which is one of the hereditary sensory and autonomic neuropathies (HSAN). Loss of pain, fever due to anhidrosis, recurrent fractures, chronic osteomyelitis, mental retardation, self mutilation, wound ulcers can be seen. We present a 10-year-old boy with loss of generalized pain sensation, chronic osteomyelitis on his right distal femur, bilateral corneal opacities, and decreased mental capacity.
dc.language.isoeng
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectInternal Medicine
dc.subjectAssessment and Diagnosis
dc.subjectMedicine (miscellaneous)
dc.subjectGeneral Medicine
dc.subjectHealth Sciences
dc.subjectTemel Tıp Bilimleri
dc.subjectFamily Practice
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleCongenital Insensitivity to Pain with Anhidrosis (CIPA) Manifested with Chronic Osteomyelitis; A Case Report
dc.typeMakale
dc.relation.journalJOURNAL OF CLINICAL AND ANALYTICAL MEDICINE
dc.contributor.departmentBezmiâlem Vakıf Üniversitesi , ,
dc.identifier.volume6
dc.identifier.issue2
dc.identifier.startpage230
dc.identifier.endpage232
dc.contributor.firstauthorID3382952


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