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[Ehlers-Danlos syndrome associated with acute pancreatitis]
A Indart1, P Zugasti, L F Alzate
1Servicio de Aparato Digestivo, Hospital de Aránzazu, San Sebastián.
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.