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Peripheral spondyloarthritis in a patient with Noonan's syndrome
Lina Maria Saldarriaga Rivera1, Elisa Fernandes de Melo1, Priscilla Damião Araujo1
1Servicio de Reumatología. Hospital Universitario Clementino Fraga Filho, Universidad Federal de Río de Janeiro (HUCFF-UFRJ), Río de Janeiro, Brasil.
Abstract:
Noonan's syndrome is an autosomal dominant genetic disorder with high phenotypic variability, characterized mainly by facial dysmorphism, congenital heart disease and short stature. We describe the case of a male patient diagnosed with Noonan's syndrome and peripheral spondyloarthritis, a previously undescribed association in the literature.
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