- Hereditary Angioneurotic Edema of the Larynx: A Case Report and Literature Review
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Shim DB, Lim YC, Shin HA, Kim JK
- KMID: 2276634
- Korean J Otolaryngol-Head Neck Surg.
- 2006 Apr;49(4):464-467.
Hereditary angioneurotic edema (HAE) is an autosomal dominant disease that results from the deficiency of C1 esterase inhibitor (C1-INH) function. Urgent proper intervention of the upper airway is warranted to... -
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- A Case of hereditary Angioedema
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Lee YS, Chung JH, Cho KH, Youn JI
- KMID: 2230849
- Korean J Dermatol.
- 1994 Feb;32(1):115-118.
We report a case of hereditary angioedema in a 48-year old female patient. She experidenced facial edema and dyspnea 5 to 6 times for a year. Similar episodes developed on... -
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- A Case of Hereditary Angioedema
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Lee JH, Cho JY, Nam DH, Hong CS
- KMID: 1662688
- Allergy.
- 1994 Dec;14(4):695-701.
Hereditary angioedema is characterized by recurrent angloedema involving any part of body especially extremities and inherited. as autosomal dominant trait. In case of laryngeal angioedema,, life-threatening result can occur, so... -
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- Efficacy of Omalizumab in a Patient with Angioedema Clinically Resembling a Hereditary Angioedema
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Kutlu A, Karabacak , Aydın E, Akarsu S, Öztürk S
- KMID: 2164648
- Ann Dermatol.
- 2016 Jun;28(3):381-382.
- doi: 10.5021/ad.2016.28.3.381
No abstract available. -
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- The First Probable Case of Hereditary Angioedema in Vietnam
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Bui Van K, Nguyen Van D
- KMID: 2167070
- Allergy Asthma Immunol Res.
- 2012 May;4(3):165-167.
- doi: 10.4168/aair.2012.4.3.165
Hereditary angioedema (HAE) is rare disorder due to C1-inhibitor deficiency (C1-INH) that are debilitating and may be life-threatening. HAE is a lack of consensus concerning diagnosis, therapy, and management, particularly... -
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- Three Cases of Hereditary Angioedema in One Family
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Suh KS, Kang JM, Kim KJ, Kang HJ
- KMID: 1863579
- Korean J Dermatol.
- 1995 Jun;33(3):564-569.
Hereditary angioedema is a rare genetic disease transmitted with a autosomal dominant trait result of a quantitative or functional defect of Cl inhibitor. We report three cases of heriditary angioedema... -
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- Angioedema due to acquired type of C1 esterase inhibitor deficiency
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Park HS
- KMID: 2252421
- Korean J Med.
- 2006 Mar;70(3):347-348.
No abstract available. -
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- A Case of Hereditary Angioedema in a 7-Year-Old Korean Girl
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Shin M, Ahn K
- KMID: 2167008
- Allergy Asthma Immunol Res.
- 2013 Jan;5(1):59-61.
- doi: 10.4168/aair.2013.5.1.59
Hereditary angioedema (HAE) is a rare autosomal dominant disease that usually occurs in adolescence and early adulthood. It is characterized by recurrent non-pitting edema involving the skin and intestinal tract,... -
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- Acquired C1 inhibitor deficiency associated with SLE
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Kang EW, Shin JY, Ryu DR, Song J, Lee WK, Park YB, Lee SK
- KMID: 2143084
- Korean J Med.
- 2001 Jul;61(1):91-94.
Acquired C1 inhibitor deficiency is a rare syndrome which usually presents with episodes of angioedema. The association of lupus erythematosus and angioneurotic edema has been previously reported but is usually... -
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- A case of hereditary angioedema not manifestated classical autosomal dominant trait
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Lee JA, Nah BG, Jun H, Seo JC, Kim MK
- KMID: 2299743
- Korean J Allergy.
- 1997 Dec;17(4):574-579.
32 year-old male patient has experienced the repeated swelling of the skin on the eyelid, both hand, foot, lower and upper extrimities and testicle spontaneously without any trauma since 17... -
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- A Case of Type 2 Hereditary Angioedema With SERPING1 Mutation
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Sim DW, Park KH, Lee JH, Park JW
- KMID: 2355900
- Allergy Asthma Immunol Res.
- 2017 Jan;9(1):96-98.
- doi: 10.4168/aair.2017.9.1.96
Hereditary angioedema is a disease of congenital deficiency or functional defect in the C1 esterase inhibitor (C1-INH) consequent to mutation in the SERPING1 gene, which encodes C1-INH. This disease manifests... -
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- Clinical experience in managing patients with hereditary angioedema in Korea: questionnaire survey and a literature review
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Lee SY, Kang HR, Jung JW, Jang GC, Lee SY, Ahn Y, Min KU, Korean Academy of Asthma, Allergy and Clinical Immunology Anaphylaxis Work Group
- KMID: 2262396
- Allergy Asthma Respir Dis.
- 2014 Sep;2(4):277-284.
- doi: 10.4168/aard.2014.2.4.277
PURPOSE: Hereditary angioedema is a familial disease which is caused by a genetic deficiency or functional defect of the C1 inhibitor, and it features episodic swelling that can affect any... -
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- A Case of Cesarean Section Delivery in a Patient with Hereditary Angioedema
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- KMID: 2299457
- Korean J Asthma Allergy Clin Immunol.
- 2012 Dec;32(4):264-267.
BACKGROUND: Hereditary angioedema is a rare disease caused by a deficiency of C1 inhibitor and inherited in an autosomal dominant manner. It leads to episodic abdominal pain and angioedema which... -
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- A Case of Melkersson-Rosenthal syndrome
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Yim JS, Jung SJ, Park WG, Lee YJ
- KMID: 1905144
- J Korean Neurol Assoc.
- 1999 Jul;17(4):602-604.
Melkersson-Rosenthal syndrome (MRS) is a rare form of hereditary angioedema characterized by a triad of orofacial swelling, relapsing facial paralysis, and a fissured tongue. However, the classic triad is not... -
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- Migraine-like Headache in a Patient with Complement 1 Inhibitor Deficient Hereditary Angioedema
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Chung JY, Kim M
- KMID: 1792989
- J Korean Med Sci.
- 2012 Jan;27(1):104-106.
- doi: 10.3346/jkms.2012.27.1.104
We report on an angioedema patient with a genetic defect in complement 1 inhibitor, manifesting migraine-like episodes of headache, effective prophylaxis with Danazol, and triptan for a treatment of acute... -
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- A Case of Lupus Nephritis Associated with Transiently Decreased C1 Inactivator Activity and Angioedema
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Oh SJ, Kang YP, Jang YB, Nam SW, Kang MJ, Lee S, Park SK, Kang SK, Kim W
- KMID: 2307245
- Korean J Nephrol.
- 2005 Sep;24(5):828-831.
C1 esterase inhibitor deficiency with consequent angioedma is an uncommon condition. Nonhereditary C1 inhibitor deficiency includes underlying disorders; lymphoproliferative disorder, autoimmune disease, hypereosinophilia, drug-induced, allergic, and idiopathic forms. The as... -
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- A Case of C1 Inhibitor Deficiency Syndrome
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Kim WH, Pahn YS, Kim NG, Oh KJ
- KMID: 2275878
- Korean J Otolaryngol-Head Neck Surg.
- 2002 Feb;45(2):191-194.
C1 inhibitor (C1 INH) deficiency is characterized by recurrent attacks of angioedema. The disorder may be inherited or acquired, with both types presenting a similar phenotypic picture. The angioedema most... -
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- A case of acquired angioedema with C1 esterase inhibitor deficiency
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Ha CY, Kim SS, Kim HJ, Han DS, Cho JW, Chung HJ, Kim HY, Nahm DH, Park HS
- KMID: 1907984
- J Asthma Allergy Clin Immunol.
- 1999 Apr;19(2):224-228.
Angioedema is a well-demarcated localized edema involving the deeper layers of the skin, including the subcutaneous tissue. Angioedema occurs with Cl esterase inhibitor (Cl INH) deficiency that may be inborn... -
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