Hereditary angioedema presenting as recurrent acute pancreatitis

Pediatrics

Volumn 137, Issue 2, 2016, Pages

  Berger, Tal D ^a   Garty, Ben Zion ^a,b  

^a SCHNEIDER CHILDREN S MEDICAL CENTER OF ISRAEL   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLASE; COMPLEMENT COMPONENT C1S INHIBITOR; COMPLEMENT COMPONENT C2; COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4; PAPAVERINE; TRIACYLGLYCEROL LIPASE; URSODEOXYCHOLIC ACID;

ABDOMINAL PAIN; ACUTE PANCREATITIS; AMYLASE BLOOD LEVEL; ANGIONEUROTIC EDEMA; ARTICLE; CASE REPORT; CHILD; CHOLECYSTECTOMY; CHOLELITHIASIS; CONSERVATIVE TREATMENT; DIFFERENTIAL DIAGNOSIS; ENDOSCOPIC ECHOGRAPHY; HUMAN; LIMB SWELLING; MALE; NAUSEA; PANCREAS DISEASE; PANCREAS ENLARGEMENT; PRESCHOOL CHILD; PRIORITY JOURNAL; RECURRENT ACUTE PANCREATITIS; TISSUE DISTRIBUTION; TRIACYLGLYCEROL LIPASE BLOOD LEVEL; URINE LEVEL; VOMITING; ACUTE DISEASE; ANGIOEDEMAS, HEREDITARY; COMPLICATION; PANCREATITIS; RECURRENT DISEASE;

ACUTE DISEASE; ANGIOEDEMAS, HEREDITARY; CHILD; HUMANS; MALE; PANCREATITIS; RECURRENCE;

EID: 84958725827     PISSN: 00314005     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.2015-0620     Document Type: Article

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