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[Antiphospholipid syndrome: a new diagnostic option in rheumatology in children. Analysis of 3 clinical cases]. / Síndrome antifosfolípido: nueva opción diagnóstica en la reumatología pediátrica. Análisis de tres casos clínicos.
Loredo-Abdalá, A; Carbajal-Rodriguez, L; Paredes-Aguilera, R; Reynés-Manzur, J.
Affiliation
  • Loredo-Abdalá A; Departamento de Medicina Interna, Instituto Nacional de Pediatría, México, D.F.
Bol Med Hosp Infant Mex ; 50(4): 265-71, 1993 Apr.
Article de Es | MEDLINE | ID: mdl-8471173
ABSTRACT
There are some patients with a clinical picture that suggests to be a rheumatological problem. However, it does not have all the criteria to be accepted such as specific problems like systemic lupus erythematosus, juvenile rheumatoid arthritis, etc. Now we know that a relation between high levels of antiphospholipid antibodies exist in these special patients and the name of the disease is antiphospholipid syndrome. This problem can be primary or secondary. This disease has been studied mainly in adults with SLE an there is not a description of this syndrome in national pediatric literature. For this reason we present three clinical cases that permit us to review both forms of the syndrome. In this way we alert want to the pediatric community about this topic, and if the number of cases increases, it will improve the knowledge and prognosis of the patients at this age.
Sujet(s)
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome des anticorps antiphospholipides Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Adolescent / Adult / Female / Humans / Infant / Male Langue: Es Journal: Bol Med Hosp Infant Mex Année: 1993 Type de document: Article
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome des anticorps antiphospholipides Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Adolescent / Adult / Female / Humans / Infant / Male Langue: Es Journal: Bol Med Hosp Infant Mex Année: 1993 Type de document: Article
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