Malignant infantile osteopetrosis: A rare cause of neonatal hypocalcemia

dc.contributor.authorKurt, Abdullah
dc.contributor.authorSen, Yasar
dc.contributor.authorElkiran, Ozlem
dc.contributor.authorAkarsu, Saadet
dc.contributor.authorKurt, A. Nese Citak
dc.contributor.authorAygun, A. Denizmen
dc.date.accessioned2026-08-12T17:13:34Z
dc.date.issued2006
dc.departmentFırat Üniversitesi
dc.description.abstractMalignant infantile osteopetrosis is a rare autosomal recessive disorder characterized by presentation in the first few months of life with manifestations relating to an underlying defect in osteoclastic bone resorption. This report describes a 10 day-old boy in whom neonatal hypocalcemia was present and whose brother had died with the diagnosis of osteopetrosis.
dc.identifier.endpage1462
dc.identifier.issn0334-018X
dc.identifier.issn2191-0251
dc.identifier.issue12
dc.identifier.orcid0000-0002-4430-444X
dc.identifier.pmid17252700
dc.identifier.scopus2-s2.0-33845988757
dc.identifier.scopusqualityQ2
dc.identifier.startpage1459
dc.identifier.urihttps://hdl.handle.net/11508/51468
dc.identifier.volume19
dc.identifier.wosWOS:000243458900012
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWalter de Gruyter Gmbh
dc.relation.ispartofJournal of Pediatric Endocrinology & Metabolism
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectmalignant infantile osteopetrosis
dc.subjecthypocalcemia
dc.subjectneonate
dc.titleMalignant infantile osteopetrosis: A rare cause of neonatal hypocalcemia
dc.typeArticle

Dosyalar