A Case Report of Aplasia Cutis Congenita Type VI: Bart Syndrome

A Case Report of Aplasia Cutis Congenita Type VI: Bart Syndrome

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 this diseases is considered a variant of aplasia...

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Bibliographic Details
Main Authors: Florica SANDRU, Catalina IORDAN, Dana ZACIU, Aida PETCA, Mihai DUMITRASCU, Adelina POPA
Format: Article
Language:English
Published: Media Med Publicis 2019-12-01
Series:Modern Medicine
Subjects:
aplasia cutis
epidermolysis bullosa
bart syndrome
genetic skin disorder
newborn
Online Access:https://medicinamoderna.ro/wp-content/uploads/2019/12/RMM_art-7-A-Case-Report-of-Aplasia-Cutis-Congenita-Type-VI-Bart-Syndrome.pdf

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https://medicinamoderna.ro/wp-content/uploads/2019/12/RMM_art-7-A-Case-Report-of-Aplasia-Cutis-Congenita-Type-VI-Bart-Syndrome.pdf

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