1.
Neurologia (Engl Ed)
; 37(3): 237-239, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35288038
2.
Neurologia
; 30(5): 315-7, 2015 Jun.
Artigo
em Inglês, Espanhol
| MEDLINE
| ID: mdl-24485591
Assuntos
Febre Familiar do Mediterrâneo/diagnóstico , Proteínas de Transporte/genética , Colchicina/uso terapêutico , Síndromes Periódicas Associadas à Criopirina/diagnóstico , Síndromes Periódicas Associadas à Criopirina/genética , Diagnóstico Diferencial , Febre Familiar do Mediterrâneo/tratamento farmacológico , Humanos , Proteína Antagonista do Receptor de Interleucina 1/uso terapêutico , Masculino , Pessoa de Meia-Idade , Proteína 3 que Contém Domínio de Pirina da Família NLR , Polirradiculoneuropatia/etiologia , Prednisona/uso terapêutico
3.
An Pediatr (Barc)
; 68(2): 143-5, 2008 Feb.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-18341881
RESUMO
Tumoral necrosis factor receptor-associated periodic syndrome (TRAPS) is an autosomal dominantly inherited disease belonging to the hereditary periodic fever syndromes, which are the main subgroup among systemic autoinflammatory diseases. TRAPS is characterized by prolonged and recurrent inflammatory attacks associated with fever and an acute phase reaction. Articular, cutaneous, ocular and abdominal symptoms may also be present. We describe the case of a 4-year-old boy with recurrent inflammatory episodes, fever and cutaneous symptoms who was diagnosed with TRAPS. We review the clinical and laboratory findings, genetic diagnosis, and treatment approach in this disease.