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 —...

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Bibliographic Details
Published in:	Bolʹ, Sustavy, Pozvonočnik
Main Authors:	N.I. Balatska, O.A. Stroi, I.V. Grynevych, P.V. Husynin, O.P. Medvedieva, K.Yu. Kyrylchuk
Format:	Article
Language:	English
Published:	Zaslavsky O.Yu. 2023-09-01
Subjects:	orphan disease ehlers-danlos syndrome dermatosparaxis type hemorrhagic syndrome case report
Online Access:	https://pjs.zaslavsky.com.ua/index.php/journal/article/view/385

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