Literature DB >> 3078778

Osteogenesis imperfecta.

R Smith.   

Abstract

It is now virtually certain that the brittle bone syndrome results from a variety of mutations in the alpha chains of type I collagen. Whilst the increasing biochemical knowledge makes prenatal diagnosis sometimes possible, the care of those with severe physical disability still provides a clinical challenge which is not always met. Future research in this disease therefore needs to be clinical as well as biochemical.

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Year:  1986        PMID: 3078778

Source DB:  PubMed          Journal:  Clin Rheum Dis        ISSN: 0307-742X


  2 in total

Review 1.  Specific entities affecting the craniocervical region: osteogenesis imperfecta and related osteochondrodysplasias: medical and surgical management of basilar impression.

Authors:  Arnold H Menezes
Journal:  Childs Nerv Syst       Date:  2008-04-10       Impact factor: 1.475

Review 2.  Syndromes with congenital brittle bones.

Authors:  Horacio Plotkin
Journal:  BMC Pediatr       Date:  2004-08-31       Impact factor: 2.125

  2 in total

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