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CAFFEY DISEASE: NEW PERSPECTIVES ON OLD QUESTIONS

The autosomal dominant form of Caffey disease is a largely self-limiting infantile bone disorder characterized by acute inflammation of soft tissues and localized thickening of the underlying bone cortex. It is caused by a recurrent arginine-to-cysteine substitution (R836C) in the α1(I) chain of typ...

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Detalhes bibliográficos
Main Authors: Nistala, Harikiran, Mäkitie, Outi, Jüppner, Harald
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3987944/
https://ncbi.nlm.nih.gov/pubmed/24389367
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2013.12.030
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