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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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Bucharest College of Physicians
2019-12-01
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| Series: | Modern Medicine |
| Subjects: | |
| 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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