A Case Report of Malignant Infantile Osteopetrosis

BACKGROUND AND OBJECTIVE: Infantile osteopetrosis is a rare genetic fetal and metabolic congenital osteo- disorder. It results from dysfunction or lack of osteoclasts. Most of patients die from anemia, bleeding and infection. The present article is a case report of malignant infantile osteopetrosis...

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Autor principal: Khorashadizadeh F, Bayani Gh, Soltani Z
Formato: article
Lenguaje:EN
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Publicado: Babol University of Medical Sciences 2011
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Acceso en línea:https://doaj.org/article/eac9990047ce4ad1ac0689e3b7701055
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spelling oai:doaj.org-article:eac9990047ce4ad1ac0689e3b77010552021-11-10T08:56:49ZA Case Report of Malignant Infantile Osteopetrosis1561-41072251-7170https://doaj.org/article/eac9990047ce4ad1ac0689e3b77010552011-09-01T00:00:00Zhttp://jbums.org/article-1-3878-en.htmlhttps://doaj.org/toc/1561-4107https://doaj.org/toc/2251-7170BACKGROUND AND OBJECTIVE: Infantile osteopetrosis is a rare genetic fetal and metabolic congenital osteo- disorder. It results from dysfunction or lack of osteoclasts. Most of patients die from anemia, bleeding and infection. The present article is a case report of malignant infantile osteopetrosis that occurred first time in Bojnord, Iran. The aim of this report is to clarify clinical manifestation of osteopetrosis, and can be helpful to diagnosis rapidly and manage sufficiently in future.CASE: A 2-month female baby with infantile osteopetrosis was referred with growth retardation, severe abdominal distention, petitia and purport. Osteopetrosis was confirmed with clinical and paraclinical examinations. She was treated with blood and PLT transfusion and discharged in good general condition.CONCLUSION: The results of this study showed that early detection and interventions can decrease mortality and morbidity in infantile osteopetrosis.Khorashadizadeh F, Bayani Gh, Soltani ZBabol University of Medical Sciencesarticlemalignant infantile osteopetrosiscase reportMedicineRMedicine (General)R5-920ENFAMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 13, Iss 5, Pp 78-82 (2011)
institution DOAJ
collection DOAJ
language EN
FA
topic malignant infantile osteopetrosis
case report
Medicine
R
Medicine (General)
R5-920
spellingShingle malignant infantile osteopetrosis
case report
Medicine
R
Medicine (General)
R5-920
Khorashadizadeh F, Bayani Gh, Soltani Z
A Case Report of Malignant Infantile Osteopetrosis
description BACKGROUND AND OBJECTIVE: Infantile osteopetrosis is a rare genetic fetal and metabolic congenital osteo- disorder. It results from dysfunction or lack of osteoclasts. Most of patients die from anemia, bleeding and infection. The present article is a case report of malignant infantile osteopetrosis that occurred first time in Bojnord, Iran. The aim of this report is to clarify clinical manifestation of osteopetrosis, and can be helpful to diagnosis rapidly and manage sufficiently in future.CASE: A 2-month female baby with infantile osteopetrosis was referred with growth retardation, severe abdominal distention, petitia and purport. Osteopetrosis was confirmed with clinical and paraclinical examinations. She was treated with blood and PLT transfusion and discharged in good general condition.CONCLUSION: The results of this study showed that early detection and interventions can decrease mortality and morbidity in infantile osteopetrosis.
format article
author Khorashadizadeh F, Bayani Gh, Soltani Z
author_facet Khorashadizadeh F, Bayani Gh, Soltani Z
author_sort Khorashadizadeh F, Bayani Gh, Soltani Z
title A Case Report of Malignant Infantile Osteopetrosis
title_short A Case Report of Malignant Infantile Osteopetrosis
title_full A Case Report of Malignant Infantile Osteopetrosis
title_fullStr A Case Report of Malignant Infantile Osteopetrosis
title_full_unstemmed A Case Report of Malignant Infantile Osteopetrosis
title_sort case report of malignant infantile osteopetrosis
publisher Babol University of Medical Sciences
publishDate 2011
url https://doaj.org/article/eac9990047ce4ad1ac0689e3b7701055
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