Arthrogryposis multiplex congenital in a child manifesting phenotypic features resembling dysosteosclerosis/osteosclerosis malformation complex; 3DCT scan analysis of the skull base

INTRODUCTION: A boy presented with arthrogryposis multiplex congenita (AMC) associated with severe central nervous system dysfunction. The clinical history and the distinctive radiographic/tomographic features were consistent but not completely diagnostic for dysosteosclerosis. CASE PRESENTATION: A...

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Detalles Bibliográficos
Autores principales: Al Kaissi, Ali, Kalchhauser, Georg, Grill, Franz, Klaushofer, Klaus
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526066/
https://www.ncbi.nlm.nih.gov/pubmed/18651947
http://dx.doi.org/10.1186/1757-1626-1-56

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526066/
https://www.ncbi.nlm.nih.gov/pubmed/18651947
http://dx.doi.org/10.1186/1757-1626-1-56

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