Publication:
Malignant Infantile Osteopetrosis with Bone Marrow Involvement

creativeworkseries.issn1812-2027
dc.contributor.authorKhadga, M
dc.contributor.authorRahman, AZM Raihanur
dc.contributor.authorBenzamin, Md
dc.contributor.authorAhamed, N
dc.contributor.authorAkter, S
dc.contributor.authorNahid-E-Subha
dc.contributor.authorHasan, M
dc.contributor.authorKhan, LN
dc.contributor.authorRukunuzzaman,Md
dc.date.accessioned2025-12-22T09:16:03Z
dc.date.available2025-12-22T09:16:03Z
dc.date.issued2022
dc.descriptionKhadga M, AZM Raihanur Rahman, Md Benzamin, Ahamed N, Akter S, Nahid-E-Subha, Hasan M, Khan LN, Md Rukunuzzaman Department of Pediatric Gastroenterology and Nutrition Bangabandhu Sheikh Mujib Medical University (BSMMU) Dhaka, Bangladesh
dc.description.abstractABSTRACT Osteopetrosis (Marble bone disease) is a very rare congenital genetic disease of skeleton, resulting from defective bone resorption, due to functionally defective osteoclast, leading to accumulation of excessive bone mass. Malignant infantile osteopetrosis (MIO) is one of the varieties of osteopetrosis, which is fatal and is diagnosed in early infancy. Malignant infantile osteopetrosis is present with abnormal bone remodeling, hematological abnormities, features of extramedullary hematopoiesis. Radiology is the key of diagnosis. In this case, we present a 5-month- old male infant diagnosed as malignant infantile osteopetrosis, who presented with bronchopneumonia, anemia, thrombocytopenia, hepatosplenomegaly, failure to thrive (FTT). KEY WORDS Fatal, Genetic, Malignant infantile osteopetrosis
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3797
dc.language.isoen_US
dc.publisherKathmandu University
dc.subjectFatal
dc.subjectGenetic
dc.subjectMalignant infantile osteopetrosis
dc.titleMalignant Infantile Osteopetrosis with Bone Marrow Involvement
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage110
oaire.citation.startPage107
relation.isJournalIssueOfPublicationf6ab97c3-6b6b-4175-bdcf-2dd1ced41610
relation.isJournalIssueOfPublication.latestForDiscoveryf6ab97c3-6b6b-4175-bdcf-2dd1ced41610
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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