Erythema marginatum as an early symptom of hereditary angioedema: Case report of 2 newborns

Pediatrics

Volumn 137, Issue 2, 2016, Pages

  Martinez Saguer, Inmaculada ^a   Farkas, Henriette ^b  

^a Hemophilia Center Rhine Main GmbH   (Germany)

^b SEMMELWEIS UNIVERSITY   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN; ARGININE; COMPLEMENT COMPONENT C1S INHIBITOR; CYSTEINE; DANAZOL; ICATIBANT; TRANEXAMIC ACID;

ABDOMINAL BULGE; ADOLESCENT; ADULT; ARTICLE; AWARENESS; C1 INHIBITOR DEFICIENCY HEREDITARY ANGIOEDEMA; CASE REPORT; CHILD; CONTROLLED STUDY; ECHOGRAPHY; ERYTHEMA MARGINATUM; FAMILY HISTORY; FEMALE; GENETIC DISORDER; HUMAN; INFANT; LARYNX EDEMA; MISSENSE MUTATION; NEWBORN; OVARY CYST; PRIORITY JOURNAL; PRODROMAL SYMPTOM; PROTEIN BLOOD LEVEL; RASH; RECOGNITION; RECURRENT DISEASE; SWELLING; COMPLICATION; ERYTHEMA; HEREDITARY ANGIOEDEMA TYPES I AND II;

ERYTHEMA; FEMALE; HEREDITARY ANGIOEDEMA TYPES I AND II; HUMANS; INFANT, NEWBORN;

EID: 84958725325     PISSN: 00314005     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.2015-2411     Document Type: Article

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