Physician- and patient-reported dermatologic comorbidities of hypermobile Ehlers-Danlos syndrome - 20/03/24
Doi : 10.1016/j.jaad.2023.11.036
Alan N. Snyder, MD, MSCR a, ⁎ 
, Almeera Lateef, BS b, Nicholas Strat, MSCR a, Laura Andrews, MD, MSCR a, Chelsea Shope, MD, MSCR a, Cortney Gensemer, PhD c, Bao Xin Liang, BS d, Taylor Petrucci, MS c, Mark Lavallee, MD e, Russel Norris, PhD c, Dirk Elston, MD a
, Almeera Lateef, BS b, Nicholas Strat, MSCR a, Laura Andrews, MD, MSCR a, Chelsea Shope, MD, MSCR a, Cortney Gensemer, PhD c, Bao Xin Liang, BS d, Taylor Petrucci, MS c, Mark Lavallee, MD e, Russel Norris, PhD c, Dirk Elston, MD a a Department of Dermatology and Dermatologic Surgery, Medical University of South Carolina, Charleston, South Carolina
b College of Medicine, Medical University of South Carolina, Charleston, South Carolina
c Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, South Carolina
d John A. Burns School of Medicine, University of Hawai’i, Honolulu, Hawai’I
e Department of Orthopedics, University of Pittsburgh Medical Center, Central PA, Harrisburg, Pennsylvania
∗Correspondence to: Alan N. Snyder, MD, MSCR, 171 Ashley Avenue, Charleston, SC 29425171 Ashley AvenueCharlestonSC29425
Key words : connective tissue disease, Ehlers-Danlos syndrome
| Funding sources: This work was supported by Ehlers Danlos Society (RAN), and the Maltz Foundation (RAN). |
|
| IRB approval status: Not applicable. |
© 2023
American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 90 - N° 4
P. 824-826 - avril 2024 Retour au numéro
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