1.
Rev Esp Enferm Dig
; 88(1): 43-5, 1996 Jan.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-8616001
RESUMO
Ehlers-Danlos syndrome type IV is a heritable disease of type III collagen metabolism. Most patients have a defect either in the synthesis or structure of type III procollagen, a finding consistent with the fact that these patients are prone to spontaneous rupture of the aorta and intestines, tissues rich in type III collagen. The diagnosis is suspected in a patient with a combination of clinical manifestations and family history, but it is confirmed only by culture of the patient's skin fibroblasts and the demonstration of a defect in type III collagen metabolism. We present a patient with Ehlers-Danlos type IV syndrome who developed a recurrent colon perforation, and discuss the surgical strategy to prevent recurrences.
Assuntos
Síndrome de Ehlers-Danlos/complicações , Perfuração Intestinal/etiologia , Doenças do Colo Sigmoide/etiologia , Adulto , Colo Sigmoide/patologia , Síndrome de Ehlers-Danlos/patologia , Feminino , Humanos , Perfuração Intestinal/patologia , Perfuração Intestinal/cirurgia , Recidiva , Doenças do Colo Sigmoide/patologia , Doenças do Colo Sigmoide/cirurgia
2.
Rev Esp Enferm Apar Dig
; 71(4): 299-304, 1987 Apr.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-3602563
3.
Rev Esp Enferm Apar Dig
; 65(2): 171-6, 1984 Feb.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-6739937
4.
Rev Esp Enferm Apar Dig
; 44(6): 563-74, 1974 Nov 15.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-4438785
5.
Rev Esp Enferm Apar Dig
; 44(4): 387-400, 1974 Oct 15.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-4438773
6.
Rev Esp Enferm Apar Dig
; 43(2): 165-76, 1974 Mar 15.
Artigo
em Espanhol
| MEDLINE
| ID: mdl-4840485