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Protein-losing enteropathy in camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome
BACKGROUND: Camptodactyly-arthropathy-coxa vara-pericarditis (CACP, OMIM: #208250) syndrome is a rare autosomal recessive disease that can be difficult to recognise not only because of its wide clinical variability but also because of its clinical resemblance to juvenile idiopathic arthritis (JIA)....
Autores principales: | Peters, Bram, Schuurs-Hoeijmakers, Janneke H. M., Fuijkschot, Joris, Reimer, Annette, van der Flier, Michiel, Lugtenberg, Dorien, Hoppenreijs, Esther P.A.H. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880819/ https://www.ncbi.nlm.nih.gov/pubmed/27224999 http://dx.doi.org/10.1186/s12969-016-0093-5 |
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