Academic Journal

Reproductive alternatives for patients with dystrophic epidermolysis bullosa

التفاصيل البيبلوغرافية
العنوان: Reproductive alternatives for patients with dystrophic epidermolysis bullosa
المؤلفون: Denise Maria Christofolini, José Ricardo Magliocco Ceroni, Giovanna Guimarães Soares, Gustavo Bertollini Lamy, Ana Carolina Nemeth Calvo, Tamara Alba dos Santos, Bianca Del Bel Sonoda, Bianca Bianco, Caio Parente Barbosa
المصدر: Einstein (São Paulo), Vol 17, Iss 3
بيانات النشر: Instituto Israelita de Ensino e Pesquisa Albert Einstein.
المجموعة: LCC:Medicine
مصطلحات موضوعية: Epidermólise bolhosa distrófica, Colágeno tipo VII, Membrana basal, Hereditariedade, Aconselhamento genético, Medicine
الوصف: ABSTRACT Epidermolysis bullosa describes a group of skin conditions caused by mutations in genes encoding proteins related to dermal-epidermal adhesion. In the United States, 50 cases of epidermolysis bullosa per 1 million live births are estimated, 92% of which classified as simplex, 5% dystrophic, 1% junctional and 2% non-classified. Dystrophic epidermolysis bullosa is associated with autosomal, dominant and recessive inheritance. Epidermolysis bullosa causes severe psychological, economic and social impacts, and there is currently no curative therapy, only symptom control. Embryonic selection is available for epidermolysis bullosa patients in order to prevent perpetuation of the condition in their offspring.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
Portuguese
تدمد: 2317-6385
Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1679-45082019000300500&lng=en&tlng=en; https://doaj.org/toc/2317-6385
DOI: 10.31744/einstein_journal/2019rc4577
URL الوصول: https://doaj.org/article/ba07860856844da384e1020391c9d725
رقم الانضمام: edsdoj.ba07860856844da384e1020391c9d725
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23176385
DOI:10.31744/einstein_journal/2019rc4577