2009
DOI: 10.4103/0377-4929.54995
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Osteopetrosis: A rare cause of anemia - Review of literature

Abstract: Normocytic anaemia is caused either by hypoproliferation of haemopoietic tissue or increased destruction of red cell. Osteopetrosis is a rare cause of anaemia. The leading clinical features are pallor, growth failure, hepatosplenomegaly.On hematological examination, anemia, thrombocytopenia, leucocytosis and myelophthisic anemia are commonly observed in this disease. We are highlighting osteopetrosis as a rare cause of anemia presenting to us for evaluation of anemia.

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Cited by 6 publications
(8 citation statements)
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“…A decrease in the number of red blood cells may result in an anemia disorder. Previous literature showed a positive correlation between osteopetrosis and anemia disorder (Fischer et al, 1991;Gamsu et al, 1961;Lees and Sautter, 1979;Saluja et al, 2009;Sreehari et al, 2011). Our quantitative study of abnormal aging mice suggests that the anemia disorder may be directly linked to the internal expansion of cortical bones at diaphysis.…”
Section: Discussionmentioning
confidence: 46%
“…A decrease in the number of red blood cells may result in an anemia disorder. Previous literature showed a positive correlation between osteopetrosis and anemia disorder (Fischer et al, 1991;Gamsu et al, 1961;Lees and Sautter, 1979;Saluja et al, 2009;Sreehari et al, 2011). Our quantitative study of abnormal aging mice suggests that the anemia disorder may be directly linked to the internal expansion of cortical bones at diaphysis.…”
Section: Discussionmentioning
confidence: 46%
“…Cranial CT and MRI are additional investigations to rule out intracranial complications like cranial nerve palsies, ventriculomegaly, atrophy, tonsillar herniation, vertebral artery compression, etc., which are attributable to the skull base sclerosis. [45] Cranial CT did not reveal hydrocephalus, foraminal compression, or any other abnormalities in our infant.…”
Section: Discussionmentioning
confidence: 65%
“…AD variety also known as benign or tarda variety is detected in older children, adolescents, and adults and has a relatively benign course. [ 5 ] Infantile OP manifests in the first few months of life, usually with features of severe bone marrow failure. Clinical presentation includes hepatosplenomegaly and failure to thrive, while hematological manifestations are anemia and thrombocytopenia.…”
Section: Discussionmentioning
confidence: 99%
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“…Bone heterogeneity is an essential quantity and is affected by the composition of different bone tissues. In particular, bone composition and therefore bone heterogeneity may be affected by the process of bone turn over, bone matrix dynamics, and bone development kinetics 1315,42 . Therefore, the Nakagami parameter is a potentially useful quantity to evaluate different aspects of bone characteristics.…”
Section: Resultsmentioning
confidence: 99%