Document Detail


Capsule endoscopy findings in congenital afibrinogenemia-associated angiopathy.
MedLine Citation:
PMID:  19003752     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital afibrinogenemia is a rare genetic disorder characterized by the complete absence of functional fibrinogen. We report a 22-year-old female who developed nephrogenic arterial hypertension and intestinal ischemia due to congenital afibrinogenemia-associated angiopathy of large abdominal arteries. We describe, for the first time, the capsule findings and discuss the pathophysiology of this unusual condition.
Authors:
P Katsinelos; T Vasiliadis; K Soufleris; G Chatzimavroudis; C Zavos; G Paroutoglou; T Katsinelos; B Papaziogas; J Kountouras
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  VASA. Zeitschrift für Gefässkrankheiten     Volume:  37     ISSN:  0301-1526     ISO Abbreviation:  VASA     Publication Date:  2008 Nov 
Date Detail:
Created Date:  2008-11-12     Completed Date:  2009-01-09     Revised Date:  2012-10-19    
Medline Journal Info:
Nlm Unique ID:  0317051     Medline TA:  Vasa     Country:  Switzerland    
Other Details:
Languages:  eng     Pagination:  383-5     Citation Subset:  IM    
Affiliation:
Department of Endoscopy and Motility Unit, Central Hospital, Thessaloniki, Greece. papazio@med.auth.gr
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MeSH Terms
Descriptor/Qualifier:
Afibrinogenemia / complications*,  congenital,  pathology,  therapy
Angioplasty, Balloon
Capsule Endoscopy*
Female
Humans
Lymphangiectasis, Intestinal / etiology,  pathology
Mesenteric Artery, Superior / pathology
Mesenteric Vascular Occlusion / etiology,  pathology*,  therapy
Renal Artery Obstruction / etiology,  pathology*,  therapy
Tomography, X-Ray Computed
Young Adult

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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