Información del artículo
Resumen
El síndrome de Ehlers-Danlos es una enfermedad congénita del tejido conectivo caracterizada por laxitud articular, hiperelasticidad de la piel y fragilidad tisular. Este síndrome se caracteriza por su gran heterogeneidad clínica, genética y bioquímica, y han sido descritos varios subtipos. Describimos el caso de un paciente con la variante IV de este síndrome que desarrolló una pancreatitis aguda de forma espontánea.
Abstract
Ehlers-Danlos syndrome is an inherited connective tissue disease characterized by articular laxity, hyperelastic skin and tissue fragility. The syndrome is genetically, biochemically and clinically heterogeneous and several well-defined subtypes have been identified. We describe a patient with the type IV variant of this syndrome who developed acute spontaneous pancreatitis.
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