Acute abdominal attack of hereditary angioneurotic oedema associated with ultrasound abnormalities suggestive of acute hepatitis

Acta Paediatrica, International Journal of Paediatrics

Volumn 91, Issue 8, 2002, Pages 971-974

  Farkas, H ^a   Harmat, G ^a   Fekete, B ^a   Karadi I ^a   Visy, B ^a   Varga, L ^a  

^a SEMMELWEIS UNIVERSITY   (Hungary)

Author keywords

Ascites; C1 esterase inhibitor concentrate; Hereditary angioneurotic oedema; Sonographic liver abnormalities

Indexed keywords

COMPLEMENT COMPONENT C1S INHIBITOR;

ABDOMINAL PAIN; ACUTE HEPATITIS; ADOLESCENT; ANGIONEUROTIC EDEMA; ARTICLE; CASE REPORT; CLINICAL FEATURE; FOLLOW UP; GENETIC DISORDER; HUMAN; LIVER DISEASE; MALE; PRIORITY JOURNAL; ULTRASOUND; ACUTE ABDOMEN; ACUTE DISEASE; ECHOGRAPHY; GENETICS; HEPATITIS;

ABDOMEN, ACUTE; ACUTE DISEASE; ADOLESCENT; ANGIONEUROTIC EDEMA; CASE REPORT; HEPATITIS; HUMAN; MALE; SUPPORT, NON-U.S. GOV'T; HUMANS;

EID: 0036348089     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/080352502760148720     Document Type: Article

References (6)

1. A biochemical abnormality in hereditary angioedema: Absence of serum inhibitor of Cl esterase
2. Hereditary angioedema: Two genetic variants
3. Hereditary and acquired Cl inhibitor deficiency: Biological and chemical characteristics in 235 patients
4. Sonographic findings in abdominal hereditary angioedema
5. Sonographic appearances of the abdominal manifestations of hereditary angioedema
6. Sonography of diffuse benign liver disease: Accuracy of pattern recognition and grading