Blau syndrome: A case report of a rare granulomatous disorder
Blau syndrome is a rare condition characterized by the triad of granulomatous skin lesions, symmetric polyarthritis with boggy joint swellings, and ocular inflammation. It has an autosomal dominant mode of inheritance and occurs due to a mutation in CARD-15/NOD-2 gene which encodes the cytosolic NOD...
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Formato: | Libro |
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Wolters Kluwer Medknow Publications,
2020-01-01T00:00:00Z.
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Número de Clasificación: |
A1234.567 |
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Copia 1 | Dispoñible |