Sonographic appearances of the abdominal manifestations of hereditary angioedema

Pediatric Radiology

Volumn 31, Issue 4, 2001, Pages 296-298

  Dinkel, H P ^a   Maroske, J ^a   Schrod, L ^a  

^a UNIVERSITY OF BERN   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C1S INHIBITOR;

ABDOMEN; ABDOMINAL PAIN; ACUTE PHASE RESPONSE; ANGIONEUROTIC EDEMA; ARTICLE; ASCITES; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CLINICAL FEATURE; ECHOGRAPHY; ENTEROPATHY; FAMILY HISTORY; FEMALE; HUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PAROXYSMAL DYSPNEA; PRIORITY JOURNAL; RECURRENT DISEASE; SKIN EDEMA;

ABDOMINAL PAIN; ANGIONEUROTIC EDEMA; CHILD; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; RECURRENCE;

EID: 0035065826     PISSN: 03010449     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002470000409     Document Type: Article

References (9)

1. Gastrointestinal tract sonography
2. Hereditary and acquired C1-inhibitor deficiency: Biological and clinical characteristics in 235 patients
3. Hereditary angioedema: Its diagnostic and management perspectives
4. Hereditary angioedema: An infrequent cause of abdominal pain with ascites
5. Hereditary angioedema: The clinical syndrome and its management
6. Abdominal pain in hereditary angioedema: The role of acid hypersecretion
7. Effect of treatment with 17 alpha-alkylated androgens on C4 conversion products in hereditary angioedema studied by crossed immunoelectrophoresis
8. Angioneurotic edema of the colon
9. Hereditary angioneurotic edema of the gastrointestinal tract