Type II hereditary angioedema - Presenting as food allergy

Digestive Diseases and Sciences

Volumn 52, Issue 2, 2007, Pages 353-356

  Williams, Yvonne ^a   Byrne, Greg ^a   Lynch, Sara ^a   Feighery, Conleth ^a   Abuzakouk, Mohamed ^a  

^a ST JAMES S HOSPITAL   (Ireland)

Author keywords

Allergy; C1 inhibitor; Celiac disease; Complement deficiency; Hereditary angioedema

Indexed keywords

TRANEXAMIC ACID;

ABDOMINAL CRAMP; ADOLESCENT; ANAPHYLACTIC SHOCK; ANGIONEUROTIC EDEMA; ARTICLE; BREATHING DISORDER; CACAO; CASE REPORT; CELIAC DISEASE; FACE; FAMILY HISTORY; FEMALE; FOOD ALLERGY; HUMAN; PRIORITY JOURNAL; SWELLING; VOMITING;

ADOLESCENT; ANGIONEUROTIC EDEMA; CELIAC DISEASE; COMPLEMENT C1 INACTIVATOR PROTEINS; DIAGNOSIS, DIFFERENTIAL; FEMALE; FOOD HYPERSENSITIVITY; HUMANS; MUTATION, MISSENSE; PEDIGREE; RECURRENCE; SERPINS;

EID: 33846829930     PISSN: 01632116     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10620-006-9294-y     Document Type: Article

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