Síndrome camptodactilia-artropatia-coxa-vara-pericardite: revisão bibliográfica
DOI:
https://doi.org/10.11606/issn.2317-0190.v31iSupl.1a225168Palavras-chave:
Artropatias, Doenças Raras, Coxa VaraResumo
A síndrome camptodactilia-artropatia-coxa-vara-pericardite (CACP) é uma doença ocasionada pelas mutações no gene proteoglicano 4 (PRG4), codificador da glicoproteína Lubricina. Esta substância tem função de lufricar as estruturas articulares e, assim, evitar a deterioração progressiva devido seu papel condoprotetor.
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