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Updated: Jul 11, 2025

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
[Hereditary epidermolysis bullosa in children]
Nathalia Bellon1, Isabelle Corset1
1Service de dermatologie, hôpital Necker-Enfants malades, AP-HP, Centre de référence des maladies rares de la peau et des muqueuses d'origine génétique (Magec), 149 rue de Sèvres, 75015 Paris, France.
Abstract:
Hereditary epidermolysis bullosa (HES) is a heterogeneous group of rare genetic disorders characterized by localized or generalized fragility of the skin and/or mucous membranes, varying greatly in severity from one form to another and even within a subgroup. Skin wounds can be a source of pain, pruritus and discomfort from birth. Progression varies from patient to patient and from form to form. Specific care must be provided from the neonatal period onwards, and throughout life, to aid healing and limit complications. Nurses are at the heart of skin care for HES patients, and must be familiar with the main principles, while adapting to the individual.
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