Literature DB >> 9227748

Clinical signs and diagnosis of osteogenesis imperfecta in three dogs.

B G Campbell1, J A Wootton, L Krook, J DeMarco, R R Minor.   

Abstract

When a young dog is evaluated for multiple fractures with minimal to no accompanying trauma, the primary differential diagnoses are metabolic disease, physical abuse, and osteogenesis imperfecta (OI). Of these, secondary hyperparathyroidism is most common, but if serum concentrations of ionized calcium, phosphorus, vitamin D, and parathormone are within reference ranges, OI must be considered. Osteogenesis imperfecta is a heritable disease characterized by brittle bones. Results of studies using cultured skin fibroblasts indicate that most cases of OI in human beings are caused by a mutation in a type-I collagen gene. Osteogenesis imperfecta was recently identified in 3 dogs. Radiographic findings included multiple fractures in various stages of healing and generalized osteopenia. Cultured fibroblasts from skin biopsy specimens were used to diagnose OI. Structural abnormalities were found in type-I collagen from each dog. This cell culture assay can be used to evaluate dogs with brittle bones.

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Year:  1997        PMID: 9227748

Source DB:  PubMed          Journal:  J Am Vet Med Assoc        ISSN: 0003-1488            Impact factor:   1.936


  2 in total

1.  Suspect osteogenesis imperfecta in a male kitten.

Authors:  Michelle D Evason; Susan M Taylor; Trevor N Bebchuk
Journal:  Can Vet J       Date:  2007-03       Impact factor: 1.008

Review 2.  Animal models of osteogenesis imperfecta and related syndromes.

Authors:  Agnès S Kamoun-Goldrat; Martine F Le Merrer
Journal:  J Bone Miner Metab       Date:  2007-06-25       Impact factor: 2.976

  2 in total

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