Epidermolysis bullosa

Epidermolysis bullosa (EB) is a hereditary multisystemic disease caused by genetic defects in the skin's structural proteins. Depending on the type of disease, symptoms vary from localised fragility and bullae to a widespread generalised form, including extracutaneous manifestations. In the mos...

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Main Authors: Anđelić Slađana, Stefanović Ivana, Tasić-Uroš Danijela, Milivojčević- Bevc Ivana, Savić Nikola
Format: Article
Language:English
Published: City Medical emergency department, Belgrade 2024-01-01
Series:Halo 194
Subjects:
Online Access:https://scindeks-clanci.ceon.rs/data/pdf/2334-6477/2024/2334-64772402061A.pdf
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author Anđelić Slađana
Stefanović Ivana
Tasić-Uroš Danijela
Milivojčević- Bevc Ivana
Savić Nikola
author_facet Anđelić Slađana
Stefanović Ivana
Tasić-Uroš Danijela
Milivojčević- Bevc Ivana
Savić Nikola
author_sort Anđelić Slađana
collection DOAJ
description Epidermolysis bullosa (EB) is a hereditary multisystemic disease caused by genetic defects in the skin's structural proteins. Depending on the type of disease, symptoms vary from localised fragility and bullae to a widespread generalised form, including extracutaneous manifestations. In the most severe forms, EB causes death in the earliest period of life. The treatment of EB is complex and usually requires the involvement of several different specialists. Without curative therapy, treatment is oriented towards supportive care, symptom control, and preventing mild to severe complications. Vector gene therapy Vyjuvek (beremagene geperpavec), based on the herpes simplex virus type 1, is a new hope for treating wounds in patients older than six months who suffer from dystrophic forms of EB.
format Article
id doaj-art-f60c63c102aa4129ac6b475a347d6c62
institution Kabale University
issn 2334-6477
language English
publishDate 2024-01-01
publisher City Medical emergency department, Belgrade
record_format Article
series Halo 194
spelling doaj-art-f60c63c102aa4129ac6b475a347d6c622025-02-05T13:08:55ZengCity Medical emergency department, BelgradeHalo 1942334-64772024-01-01302617010.5937/halo30-519032334-64772402061AEpidermolysis bullosaAnđelić Slađana0https://orcid.org/0000-0002-5233-8287Stefanović Ivana1https://orcid.org/0009-0004-4064-3577Tasić-Uroš Danijela2https://orcid.org/0009-0006-5419-9758Milivojčević- Bevc Ivana3https://orcid.org/0009-0007-1346-126XSavić Nikola4https://orcid.org/0000-0002-6687-9455Zavod za urgentnu medicinu, Beograd, SerbiaZavod za urgentnu medicinu, Beograd, SerbiaZavod za urgentnu medicinu, Beograd, SerbiaZavod za urgentnu medicinu, Beograd, SerbiaUniverzitet Singidunum, Fakultet zdravstvenih i poslovnih studija, Valjevo, SerbiaEpidermolysis bullosa (EB) is a hereditary multisystemic disease caused by genetic defects in the skin's structural proteins. Depending on the type of disease, symptoms vary from localised fragility and bullae to a widespread generalised form, including extracutaneous manifestations. In the most severe forms, EB causes death in the earliest period of life. The treatment of EB is complex and usually requires the involvement of several different specialists. Without curative therapy, treatment is oriented towards supportive care, symptom control, and preventing mild to severe complications. Vector gene therapy Vyjuvek (beremagene geperpavec), based on the herpes simplex virus type 1, is a new hope for treating wounds in patients older than six months who suffer from dystrophic forms of EB.https://scindeks-clanci.ceon.rs/data/pdf/2334-6477/2024/2334-64772402061A.pdfepidermolysis bullosaclinical presentationtherapytreatmentvyuvek
spellingShingle Anđelić Slađana
Stefanović Ivana
Tasić-Uroš Danijela
Milivojčević- Bevc Ivana
Savić Nikola
Epidermolysis bullosa
Halo 194
epidermolysis bullosa
clinical presentation
therapy
treatment
vyuvek
title Epidermolysis bullosa
title_full Epidermolysis bullosa
title_fullStr Epidermolysis bullosa
title_full_unstemmed Epidermolysis bullosa
title_short Epidermolysis bullosa
title_sort epidermolysis bullosa
topic epidermolysis bullosa
clinical presentation
therapy
treatment
vyuvek
url https://scindeks-clanci.ceon.rs/data/pdf/2334-6477/2024/2334-64772402061A.pdf
work_keys_str_mv AT anđelicslađana epidermolysisbullosa
AT stefanovicivana epidermolysisbullosa
AT tasicurosdanijela epidermolysisbullosa
AT milivojcevicbevcivana epidermolysisbullosa
AT savicnikola epidermolysisbullosa