1.
Gastroenterol Hepatol
; 24(1): 13-5, 2001 Jan.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-11219134
RESUMO
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.