PedAM

Pediatric Disease Annotations & Medicines

Disease	angioedema
Phenotype	C0019243\|c1 inhibitor deficiency
Sentences	16
PubMedID- 25054967	Context and objective: hereditary angioedema (hae) with c1 inhibitor deficiency manifests as recurrent episodes of edema involving the skin, upper respiratory tract and gastrointestinal tract.
PubMedID- 23282382	The prognosis for patients with acquired angioedema associated with c1 inhibitor deficiency is variable and depends on control of the underlying disorder.
PubMedID- 26429506	The safety of treatments for angioedema with hereditary c1 inhibitor deficiency.
PubMedID- 24556385	Methods: eleven patients (nine hae type 1, one hae type 2 and one acquired angioedema with c1 inhibitor deficiency) received between one and six, mostly self-administered, doses of rhc1inh for acute hae attacks.
PubMedID- 25924832	Background: attacks of hereditary angioedema with c1 inhibitor deficiency (c1-inh-hae) are commonly treated in the emergency department.
PubMedID- 26154504	Hereditary angioedema with c1 inhibitor deficiency (c1-inh-hae) is a rare autosomal dominant disease with an uncertain prevalence estimated to be 1: 50 000 [1] and is caused by mutation in the serping1 gene.
PubMedID- 25538858	In this review, we describe known mechanisms for the development of angioedema in patients with c1 inhibitor deficiency.
PubMedID- 24054366	Hereditary angioedema with c1 inhibitor deficiency: clinical presentation and quality of life of 193 french patients.
PubMedID- 20804470	Mutational spectrum and phenotypes in danish families with hereditary angioedema because of c1 inhibitor deficiency.
PubMedID- 22230421	Acquired angioedema with c1 inhibitor deficiency associated with anticardiolipin antibodies.
PubMedID- 20859548	Hereditary angioedema, resulting from inherited partial c1 inhibitor deficiency, is a disabling condition characterized by intermittent episodes of bradykinin-mediated angioedema.
PubMedID- 23937903	Hereditary angioedema with c1 inhibitor deficiency: delay in diagnosis in europe.
PubMedID- 22909164	Background: hereditary angioedema (hae) owing to c1 inhibitor deficiency is an autosomal dominant disorder, characterized by recurrent, potentially life-threatening, localized attacks of tissue swelling.
PubMedID- 24970460	Acquired angioedema with c1 inhibitor deficiency secondary to splenic marginal zone b-cell lymphoma.
PubMedID- 21039598	Standard care impact on angioedema because of hereditary c1 inhibitor deficiency: a 21-month prospective study in a cohort of 103 patients.
PubMedID- 22126399	Evidence-based recommendations for the therapeutic management of angioedema owing to hereditary c1 inhibitor deficiency: consensus report of an international working group.

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