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Hereditary Angioedema: Transforming Rare Disease Care with Targeted Therapies
Hereditary Angioedema (HAE) is a rare, potentially life-threatening genetic disorder characterized by recurrent, unpredictable swelling episodes affecting the skin, gastrointestinal tract, and airway. It is caused by deficiencies or dysfunction of C1 esterase inhibitor (C1-INH), leading to excessive bradykinin production—a key mediator of vascular permeability. Advances in targeted...
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