Hereditary angioedema - A forgotten cause of the 'medical' acute abdomen [6]

International Journal of Colorectal Disease

Volumn 22, Issue 11, 2007, Pages 1415-1416

  Baraza, Wal ^a,b   Garner, J P ^a   Amin, S N ^a  

^a NORTHERN GENERAL HOSPITAL   (United Kingdom)

^b NONE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C1S INHIBITOR;

ABDOMINAL TENDERNESS; ACUTE ABDOMEN; ADULT; ANGIONEUROTIC EDEMA; ASCITES; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; DIFFERENTIAL DIAGNOSIS; EPIGASTRIC PAIN; FEMALE; GASTROESOPHAGEAL REFLUX; HOSPITAL ADMISSION; HOSPITAL DISCHARGE; HUMAN; LETTER; LEUKOCYTOSIS; MALE; METABOLIC ACIDOSIS; PRIORITY JOURNAL; TACHYCARDIA; ULCER PERFORATION; UPPER ABDOMINAL PAIN; VOMITING;

ABDOMEN, ACUTE; ADULT; ANGIOEDEMA, HEREDITARY; COMPLEMENT C1 INHIBITOR PROTEIN; EDEMA; FEMALE; HUMANS; MALE; TOMOGRAPHY, X-RAY COMPUTED;

EID: 34648835169     PISSN: 01791958     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00384-006-0201-y     Document Type: Letter

References (0)