A pseudohypoparathyroidism case with rarely seen intracranial calcification in childhood

dc.contributor.authorKorkmaz, Ozlem
dc.contributor.authorGursu, Hazim Alper
dc.contributor.authorKaya, Ali
dc.contributor.authorAldemir, Betul Aslaner
dc.date.accessioned2024-10-26T18:04:16Z
dc.date.available2024-10-26T18:04:16Z
dc.date.issued2014
dc.departmentSivas Cumhuriyet Üniversitesi
dc.description.abstractIntroduction: Pseudohypoparathyroidism (PHPT) is characterized with end-organ resistance to parathormone (PTH) although normal hormone secretion. It is divided into two groups as Type 1 and Type 2. Furthermore, Type 1 PHPT is subdivided into 3 subgroups as 'a', 'b' and 'c'. Case: A 10-year-old male patient was admitted to our department with numbness and spasm in hands and we have detected hypocalcemia, hyperphosphatemia and increased parathormone levels. Cranial computed tomography revealed patchy calcific areas in phenotypically normal case. Conclusion: We primarily considered the case as having PHPT Type 1b or Type 2 and started active vitamine D and calcium replacement therapies which improved clinical and laboratory findings.
dc.identifier.doi10.5222/buchd.2014.214
dc.identifier.endpage217
dc.identifier.issn2146-2372
dc.identifier.issn1309-9566
dc.identifier.issue3
dc.identifier.startpage214
dc.identifier.urihttps://doi.org/10.5222/buchd.2014.214
dc.identifier.urihttps://hdl.handle.net/20.500.12418/28844
dc.identifier.volume4
dc.identifier.wosWOS:000420515800012
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isotr
dc.publisherDr Behcet Uz Cocuk Hastaliklari Ve Cerrahisi
dc.relation.ispartofIzmir Dr Behcet Uz Cocuk Hastanesi Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjecthypocalcemia
dc.subjectparathormon
dc.subjectcalcification
dc.titleA pseudohypoparathyroidism case with rarely seen intracranial calcification in childhood
dc.typeArticle

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