Dermatosparaxis type of Ehlers-Danlos syndrome: case report
Background. The dermatosparaxial type of Ehlers-Danlos syndrome (EDSDERMS, VIIC, dEDS) is an extremely rare disorder. To date, 15 patients with this type of Ehlers-Danlos syndrome are known worldwide. The purpose was to improve knowledge and spread data about the orphan connective tissue disease —...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Zaslavsky O.Yu.
2023-09-01
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Series: | Bolʹ, Sustavy, Pozvonočnik |
Subjects: | |
Online Access: | https://pjs.zaslavsky.com.ua/index.php/journal/article/view/385 |