No cure; management involves preventing and treating swelling episodes; medications can be effective in controlling symptoms, allowing individuals with hereditary angioedema to lead normal lives
Hereditary angioedema is a genetic disorder characterized by episodes of severe swelling, often affecting the face and throat. It is caused by a deficiency or dysfunction of a certain protein. Management includes medications to prevent and treat episodes and support during acute attacks.
Genetic disorder causing episodes of severe swelling, often in the face, throat, and abdomen
Recurrent episodes of swelling (angioedema), abdominal pain, difficulty breathing
Clinical evaluation, sometimes blood tests
Generally good with appropriate management
Swelling episodes, complications affecting daily life
Genetic mutations affecting the C1 inhibitor gene, leading to uncontrolled activation of certain proteins in the body
Medications (C1 inhibitor replacement, bradykinin receptor antagonists), management of triggers and symptoms
Medications (C1 inhibitor replacement, bradykinin receptor antagonists), management of triggers and symptoms
Genetic disorder causing recurrent episodes of swelling
Medications, supportive care
As always, consult with healthcare professionals for personalized advice and care.
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