Literature DB >> 9531912

Osteopetrosis.

J Carolino1, J A Perez, A Popa.   

Abstract

Osteopetrosis is a rare hereditary bone disorder that presents in one of three forms: osteopetrosis tarda, osteopetrosis congenita and "marble bone" disease. Osteopetrosis tarda, the benign form, presents in adulthood, while the two more malignant variants, osteopetrosis congenita and marble bone disease, present in infancy and childhood, respectively. In all three forms, the main features are pathologic alteration of osteoclastic bone resorption and thickening of cortical and lamellar bones. Osteopetrosis tarda is usually discovered accidentally on routine radiographs and is often asymptomatic; however, patients may present because of related degenerative joint disease. Osteopetrosis congenita results in bone marrow failure and is almost always fatal. Marble bone disease causes short stature, cerebral calcification and mental retardation. Bone marrow transplant is the only chance for survival in patients with osteopetrosis congenita.

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Mesh:

Year:  1998        PMID: 9531912

Source DB:  PubMed          Journal:  Am Fam Physician        ISSN: 0002-838X            Impact factor:   3.292


  4 in total

1.  The failure experience of complex total hip arthroplastyin osteopetrosis: case report and literature review.

Authors:  Lujue Dong; Wei He; Shaochuan Huo; Cheng Guo; Chi Zhou; Qunqun Chen; Hongyu Tang; Xinying Xie; Haibin Wang
Journal:  Int J Clin Exp Med       Date:  2015-09-15

2.  Endoscopic third ventriculostomy for the treatment of osteopetrosis-related hydrocephalus: a case-based update.

Authors:  Bhoresh Dhamija; Benedetta Ludovica Pettorini; Guirish Solanki
Journal:  Childs Nerv Syst       Date:  2011-05-07       Impact factor: 1.475

3.  Omi, a recessive mutation on chromosome 10, is a novel allele of Ostm1.

Authors:  Erika A Bosman; Jeanne Estabel; Ozama Ismail; Christine Podrini; Jacqueline K White; Karen P Steel
Journal:  Mamm Genome       Date:  2012-11-17       Impact factor: 2.957

4.  Osteomyelitis in an Osteopathia Striata with Cranial Sclerosis Patient.

Authors:  Heung-Chul Park; Hang-Gul Kim; Yong-Hwan Kim; Joo-Hwan Kim; Moon-Young Kim; Kyung-Wook Kim
Journal:  Maxillofac Plast Reconstr Surg       Date:  2014-11-12
  4 in total

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