Stem Cell Research and Regenerative Medicine

Hereditary Angiodema Journals

 Hereditary angioedema is a disorder characterized by severe swelling (angioedema) episodes that recur. The body's most common areas for developing swelling are the limbs, face, intestinal tract, and airways. Minor trauma or stress can trigger an attack, but often with no known trigger, swelling occurs. Bowel tract attacks cause extreme abdominal pain, nausea , and vomiting. Swelling in the airway can restrict breathing and lead to life-threatening obstruction of the airway. About one-third of people with this condition develop a non-itchy rash called erythema marginatum during an attack. Symptoms of hereditary angioedema typically begin in childhood and worsen during puberty. On average, untreated individuals have an attack every 1 to 2 weeks, and most episodes last for about 3 to 4 days. The frequency and duration of attacks vary greatly among people with hereditary angioedema, even among people in the same family. The journal would provide a platform for and motivate scholars, students, technologists and specialists to share their professional and academic expertise in hereditary angioedema.  

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