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)....

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Detalles Bibliográficos
Autores principales: Peters, Bram, Schuurs-Hoeijmakers, Janneke H. M., Fuijkschot, Joris, Reimer, Annette, van der Flier, Michiel, Lugtenberg, Dorien, Hoppenreijs, Esther P.A.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
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

Internet

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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