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Publikováno v:
Modern Medicine, Vol 26, Iss 4, Pp 213-217 (2019)
Bart syndrome is a genetic disorder that is characterized by the association of congenital localized absence of the skin (aplasia cutis), blister formation (epidermolysis bullosa), dystrophic nails and lesions of the mouth mucosa. The association o
Externí odkaz:
https://doaj.org/article/2ad9f65a2dc349c2a7b5d059952621fd
Autor:
Aida Petca, Dana Zaciu, Catalina Iordan, Adelina Popa, Pharmacy, Bucharest, Romania, Florica Sandru, Mihai Cristian Dumitrascu
Publikováno v:
Modern Medicine, Vol 26, Iss 4, Pp 213-217 (2019)
Bart syndrome is a genetic disorder that is characterized by the association of congenital localized absence of the skin (aplasia cutis), blister formation (epidermolysis bullosa), dystrophic nails and lesions of the mouth mucosa. The association of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f0303c3088427233377e572222408bd
https://medicinamoderna.ro/wp-content/uploads/2019/12/RMM_art-7-A-Case-Report-of-Aplasia-Cutis-Congenita-Type-VI-Bart-Syndrome.pdf
https://medicinamoderna.ro/wp-content/uploads/2019/12/RMM_art-7-A-Case-Report-of-Aplasia-Cutis-Congenita-Type-VI-Bart-Syndrome.pdf