Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3382900 | Reumatología Clínica | 2015 | 4 Pages |
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.
Keywords
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Authors
Lina Maria Saldarriaga Rivera, Elisa Fernandes de Melo, Priscilla Damião Araujo, Nelson Araujo Silva Filho, Luis Alberto Delgado Quiroz, Blanca Elena Rios Gomes Bica,