Results 191 to 200 of about 111,576 (246)

Frailty in elderly with a rare genetic disease: a geriatric score analysis in C1 inhibitor Hereditary Angioedema. [PDF]

Front Med (Lausanne)
Triggianese P, Cedola F, Barone G, Marchionni E, Mannucci L, Valentini A, Bernardini S, Novelli G, Della-Morte D.   +8 more
europepmc   +1 more source

Transmission of F12-related hereditary angioedema through a sperm donor. [PDF]

Front Immunol
Marquès L, Batlle-Masó L, Alcoceba E, Lara S, Aguiló-Cucurull A, Gil-Serrano J, Guilarte M, Colobran R.   +7 more
europepmc   +1 more source

Sebetralstat for breakthrough attacks in patients with hereditary angioedema receiving long-term prophylaxis in KONFIDENT-S. [PDF]

J Allergy Clin Immunol Glob
Kinaciyan T, Aygören-Pürsün E, Martinez-Saguer I, Soteres DF, Honda D, Manning ME, Wedner HJ, Fukunaga A, Kanarek HJ, Ohmura K, Melamed I, El-Shanawany T, Bouillet L, Lumry WR, Riedl MA, Koleilat M, Geng B, Ohsawa I, Bara N, Rehman S, Bernstein JA, Busse PJ, Cancian M, Cohn DM, Craig TJ, Farkas H, Kiani-Alikhan S, Li HH, Raasch JP, Tachdjian R, Audhya PK, Bajcic P, Chuang YH, Iverson M, Smith MD, Yea CM, Zanichelli A.   +36 more
europepmc   +1 more source

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Hereditary Angioedema

Immunology and Allergy Clinics of North America, 2022
Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder that usual results from a decreased level of functional C1-INH and clinically manifests with intermittent attacks of swelling of the subcutaneous tissue or submucosal layers of the respiratory or gastrointestinal tracts.
R Gentry, Wilkerson, Joseph J, Moellman
openaire   +3 more sources

Hereditary angioedema

Annals of Emergency Medicine, 1988
Although the condition is rare, patients with hereditary angioedema often present because of abdominal pain or airway compromise. A 27-year-old woman presented to the emergency department in acute abdominal distress. Identification of the disease in this patient allowed for proper management and avoidance of invasive procedures.
G P, Moore, W T, Hurley, S A, Pace
openaire   +2 more sources

Hereditary angioedema

Current Opinion in Pediatrics, 2005
Major advances have been made in understanding the clinical signs and symptoms, the pathophysiology and the treatment of hereditary angioedema. This disease that often begins in childhood is caused by partial absence of the plasma protein C1-inhibitor.
openaire   +4 more sources

Hereditary Angioedema and Pregnancy

Obstetric Anesthesia Digest, 2009
Background:  Hereditary angioedema (HAE) is an autosomal dominant disease caused by a quantitative or functional defect in C1‐esterase inhibitor (C1‐INH). Patients with this deficiency present with episodes of angioedema which can be life‐threatening. Studies examining HAE and pregnancy are scarce with little known about the interrelationship between ...
Niranthari, Chinniah, Constance H, Katelaris   +1 more
openaire   +2 more sources

Review of hereditary angioedema

LymphoSign Journal, 2016
Hereditary angioedema (HAE) is a rare disease caused by deficiency of C1 esterase inhibitor (C1-INH). It is an autosomal dominant disease caused by a variety of mutations in the C1-INH gene. C1-INH is an important regulator of several pathways. One pathway it affects is the kallikrein–kinin pathway, which results in the generation of bradykinin ...
Lisa W. Fu, Tamlyn Freedman-Kalchman, Stephen Betschel, Gordon Sussman   +3 more
openaire   +1 more source

Hereditary Angioedema in Pregnancy

Obstetrical & Gynecological Survey, 2021
Importance Hereditary angioedema is a rare disease of potentially life-threatening attacks of angioedema that can affect patients of all ages, including women of childbearing age. Pregnancy can affect the course of the disease and the choice of treatment used. It is important for the care providers to recognize this disease and
Irene I, Chair, Karen E, Binkley, Stephen D, Betschel   +2 more
openaire   +2 more sources