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Arthrogryposis multiplex congenita in a child with congenital fractures: a case report
BACKGROUND: Bruck syndrome is an exceedingly rare form of osteogenesis imperfecta, inherited autosomal recessively and presenting with the concurrence of bone fragility and congenital contractures of large joints. The disease usually progresses relentlessly to result in recurrent fractures, short st...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9579550/ https://www.ncbi.nlm.nih.gov/pubmed/36258204 http://dx.doi.org/10.1186/s13256-022-03587-1 |