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Hereditary angioedema in a family.
Article ي En | IMSEAR | ID: sea-91777
Hereditary angioedema is an uncommon clinical condition. Life-long episodic brawny and non-itchy swelling of the extremities, face and trunk, with episodic abdominal pain and familial occurrence are the typical features. Oedema causing obstruction of airways may lead to suffocation and even death. The diagnosis can be confirmed by finding low levels of C1 esterase inhibitor, C4 and C2. Therapy with synthetic androgenic agents can ameliorate the condition to a large extent.
الموضوعات
النص الكامل: 1 الفهرس: IMSEAR الموضوع الرئيسي: Female / Humans / Male / Child / Chromosome Aberrations / Adolescent / Adult / Chromosome Disorders / Danazol / Genes, Dominant اللغة: En السنة: 1992 نوع: Article
النص الكامل: 1 الفهرس: IMSEAR الموضوع الرئيسي: Female / Humans / Male / Child / Chromosome Aberrations / Adolescent / Adult / Chromosome Disorders / Danazol / Genes, Dominant اللغة: En السنة: 1992 نوع: Article