Infantile Osteopetrosis Associated With Rickets
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Yaşar Bükte 1, Fuat Gürkan 2 * , Mehmet Davutoğlu 2, Ayfer Gözü 2, Meki Bilici 2
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1 Dicle University Medical Faculty, Departments of Radiology, Diyarbakır, Turkey2 Dicle University Medical Faculty, Departments of Pediatrics, Diyarbakır, Turkey* Corresponding Author

Abstract

A 3-year-old female child was diagnosed as malignant autosomal recessive form of infantile osteopetrosis by presence of anemia, thrombocytopenia, hepatosplenomegaly, failure to thrive, visual and hearing loss, and the typical radiological images on plain radiograms. The patient had associated clinical and laboratory findings of rickets as a rare presentation. Treatment with calcitriol was initiated with a short-term calcium supplement.

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Article Type: Case Report

EUR J GEN MED, 2005, Volume 2, Issue 1, 32-34

https://doi.org/10.29333/ejgm/82263

Publication date: 15 Jan 2005

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Article Downloads: 821

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