veterinary junctional epidermolysis bullosa
épidermolyse bulleuse jonctionnelle vétérinaire
junctional epidermolysis bullosa oor Frans
junctional epidermolysis bullosa
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épidermolyse bulleuse jonctionnelle
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Human disease
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The anaesthetic management of two children with junctional epidermolysis bullosa, formerly called the letalis form, is described.
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Namely, a drug to be used in gene therapy for recessively transmitted genetic disease containing an immunosuppressant and a gene responsible for a recessively transmitted genetic disease such as recessively transmitted trophic congenital epidermolysis bullosa, junctional congenital epidermolysis bullosa, hemidesmosomal congenital epidermolysis bullosa or congenital ichthyosis is prepared.
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These studies should target LAMA3 and other genes involved in JEB too. Junctional epidermolysis bullosa.
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I have been living with Junctional Epidermolysis Bullosa (JEB) for 32 years.
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Charlene is 25 and suffers from non-Herlitz junctional epidermolysis bullosa.
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Also, the causal mutation responsible for junctional epidermolysis bullosa (JEB) in France draft horse breeds was search.
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Interview of Charlene, who suffers from junctional epidermolysis bullosa
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JEB is short for Junctional Epidermolysis Bullosa.
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Four big categories characterize this group, which includes epidermolysis bullosa simplex, dystrophic epidermolysis bullosa, junctional epidermolysis bullosa, and to a certain extent, Kindler’s syndrome.
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Junctional epidermolysis bullosa (JEB)– appearing at birth and generally more severe than EB Simplex, Junctional EB presents with blisters at the site of friction. This type affects laminin and collagen.
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Baby Shea was born on December 9, 2013 and was diagnosed with an extremely rare genetic disorder called Junctional Epidermolysis Bullosa, in which a missing protein prevents the attachment of the outer layer of skin to the deeper layer of skin tissue.
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Form of epidermolysis bullosa characterized by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IgG deposited at the dermo-epidermal junction.
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Epidermolysis bullosa Epidermolysis bullosa is characterized by a problem of junction between the epidermis and the dermis, which results in a bullous detachment and a skin abrasion.
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Epidermolysis bullosa is characterized by a problem of junction between the epidermis and the dermis, which results in a bullous detachment and a skin abrasion.
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Hereditary epidermolysis bullosa are rare diseases, due to mutations of genes encoding structural proteins of the dermal-epidermal junction.
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