HEREDITARY ANGIOEDEMA: MISDIAGNOSIS, MISMANAGEMENT AND REPORT OF SEVEN CASES FROM A FAMILY

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GHAFFARI JAVAD; REZAEI MOHAMMADSADEGH; BAHARI AMIR

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Journal Paper

Paper Information

Journal: JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES Year:2013 | Volume:22 | Issue:97 Page(s): 283-288

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Title

HEREDITARY ANGIOEDEMA: MISDIAGNOSIS, MISMANAGEMENT AND REPORT OF SEVEN CASES FROM A FAMILY

Author(s)

GHAFFARI JAVAD | REZAEI MOHAMMADSADEGH | BAHARI AMIR | Issue Writer Certificate

Keywords

HEREDITARY ANGIOEDEMAQ2

COMPLEMENTQ4

DIAGNOSISQ3

COMPLICATIONQ3

Abstract

HEREDITARY ANGIOEDEMA is a rare disorder of COMPLEMENT system which is often seen with autosomal dominant hereditary. Clinical characteristics include non- pruritic and non-pitting mucocutaneous edema that could involve all parts of the body. This study reports seven cases of HEREDITARY ANGIOEDEMA with classical manifestations accompanied by low function of C1INH (type 2). One death occurred due to laryngeal edema. This case study aimed at increasing the knowledge regarding HEREDITARY ANGIOEDEMA, its early DIAGNOSIS and correct managements.

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APA: Copy

GHAFFARI, JAVAD, REZAEI, MOHAMMADSADEGH, & BAHARI, AMIR. (2013). HEREDITARY ANGIOEDEMA: MISDIAGNOSIS, MISMANAGEMENT AND REPORT OF SEVEN CASES FROM A FAMILY. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 22(97), 283-288. SID. https://sid.ir/paper/387286/en

Vancouver: Copy

GHAFFARI JAVAD, REZAEI MOHAMMADSADEGH, BAHARI AMIR. HEREDITARY ANGIOEDEMA: MISDIAGNOSIS, MISMANAGEMENT AND REPORT OF SEVEN CASES FROM A FAMILY. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2013;22(97):283-288. Available from: https://sid.ir/paper/387286/en

IEEE: Copy

JAVAD GHAFFARI, MOHAMMADSADEGH REZAEI, and AMIR BAHARI, “HEREDITARY ANGIOEDEMA: MISDIAGNOSIS, MISMANAGEMENT AND REPORT OF SEVEN CASES FROM A FAMILY,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 22, no. 97, pp. 283–288, 2013, [Online]. Available: https://sid.ir/paper/387286/en

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