Literature DB >> 17264462

Recurrent abdominal pain due to hereditary angioedema.

Deepa Janardhanan1, Sajitha Nair, T S Subramanian.   

Abstract

Recurrent abdominal pain is a common problem in children that may need invasive procedures for diagnosis. Hereditary angioedema (HAE) is rarely considered in the differential diagnosis. Here it is reported a girl with HAE, who presented initially as recurrent abdominal pain without cutaneous manifestations. Each episode was managed elsewhere as an acute surgical emergency and an exploratory laparotomy was planned. Diagnosis was confirmed by quantitative assay of C1 inhibitor. On detailed evaluation, many members of her family were affected.

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Year:  2007        PMID: 17264462     DOI: 10.1007/s12098-007-0034-x

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   5.319


  6 in total

1.  Hereditary angioedema with recurrent abdominal pain.

Authors:  Avnish K Seth; Velu Nair; Jasjit Singh; Ved Prakash Dhand
Journal:  Indian J Gastroenterol       Date:  2002 Mar-Apr

2.  Treatment of 193 episodes of laryngeal edema with C1 inhibitor concentrate in patients with hereditary angioedema.

Authors:  K Bork; S E Barnstedt
Journal:  Arch Intern Med       Date:  2001-03-12

3.  Recurrent abdominal pain as the sole manifestation of hereditary angioedema in multiple family members.

Authors:  L B Weinstock; T Kothari; R N Sharma; S I Rosenfeld
Journal:  Gastroenterology       Date:  1987-11       Impact factor: 22.682

4.  Treatment of hereditary angioedema with a vapor-heated C1 inhibitor concentrate.

Authors:  A T Waytes; F S Rosen; M M Frank
Journal:  N Engl J Med       Date:  1996-06-20       Impact factor: 91.245

Review 5.  C1 inhibitor deficiency: consensus document.

Authors:  M M Gompels; R J Lock; M Abinun; C A Bethune; G Davies; C Grattan; A C Fay; H J Longhurst; L Morrison; A Price; M Price; D Watters
Journal:  Clin Exp Immunol       Date:  2005-03       Impact factor: 4.330

6.  Treatment of hereditary angioedema with danazol. Reversal of clinical and biochemical abnormalities.

Authors:  J A Gelfand; R J Sherins; D W Alling; M M Frank
Journal:  N Engl J Med       Date:  1976-12-23       Impact factor: 91.245

  6 in total
  3 in total

1.  Paediatric hereditary angioedema: a survey of UK service provision and patient experience.

Authors:  N Read; E Lim; M D Tarzi; P Hildick-Smith; S Burns; K J Fidler
Journal:  Clin Exp Immunol       Date:  2014-12       Impact factor: 4.330

2.  Pediatric hereditary angioedema due to C1-inhibitor deficiency.

Authors:  Henriette Farkas
Journal:  Allergy Asthma Clin Immunol       Date:  2010-07-28       Impact factor: 3.406

3.  International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

Authors:  H Farkas; I Martinez-Saguer; K Bork; T Bowen; T Craig; M Frank; A E Germenis; A S Grumach; A Luczay; L Varga; A Zanichelli
Journal:  Allergy       Date:  2016-09-08       Impact factor: 13.146

  3 in total

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