Llwytho...
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)....
Wedi'i Gadw mewn:
Cyhoeddwyd yn: | Pediatr Rheumatol Online J |
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Prif Awduron: | , , , , , , |
Fformat: | Artigo |
Iaith: | Inglês |
Cyhoeddwyd: |
BioMed Central
2016
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Pynciau: | |
Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4880819/ https://ncbi.nlm.nih.gov/pubmed/27224999 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12969-016-0093-5 |
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