Hereditary deficiency of C1-esterase inhibitor presenting with recurrent abdominal pain;He reditäres angioödem typ I durch C1-inhibitor-mangel als ursache von rezidivierenden bauchschmerzen

Klinische Padiatrie

Volumn 214, Issue 1, 2002, Pages 20-21

  Steiß, Jens Oliver ^a   Mayser, P ^b   Gortner, L ^a   Alzen, G ^c  

^a Zentrum fur Kinderheilkunde und Jugendmedizin   (Germany)

^b Zentrum fur Dermatologie und Andrologie   (Germany)

^c JUSTUS LIEBIG UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BERINERT; COMPLEMENT COMPONENT C1S INHIBITOR; DANAZOL; TRANEXAMIC ACID; UNCLASSIFIED DRUG;

ABDOMINAL PAIN; ADOLESCENT; ANGIONEUROTIC EDEMA; ARTICLE; CASE REPORT; COMPLEMENT COMPONENT C1S INHIBITOR DEFICIENCY; DIAGNOSTIC ACCURACY; DIAGNOSTIC IMAGING; EDEMA; ENZYME DEFICIENCY; FATALITY; FEMALE; GENETIC DISORDER; HAND; HUMAN; DIFFERENTIAL DIAGNOSIS; ECHOGRAPHY; GENETICS; INTESTINE OBSTRUCTION; MALE; RECURRENT DISEASE;

ABDOMINAL PAIN; ADOLESCENT; ANGIONEUROTIC EDEMA; COMPLEMENT C1 INACTIVATOR PROTEINS; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; INTESTINAL OBSTRUCTION; MALE; RECURRENCE;

EID: 0036148274     PISSN: 03008630     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-19918     Document Type: Article

References (6)

1. Hereditary angioedema with normal C1-inhibitor activity in women
2. Asphyxiation by laryngeal edema in patients with hereditary angioedema
3. Rezidivierende angioödeme dutch C1-Inhibitor-Mangel: Erstickungsrisiko
4. Untersuchungen zum hereditären Angioödem im deutschsprachigen Raum
5. Erfahrungen in der therapie des hereditären Angioödems
6. Hereditary angioedema: Its diagnostic and management perspectives