Comorbidity, misdiagnoses, and the diagnostic odyssey in patients with hypermobile Ehlers-Danlos syndrome

Author:

Halverson Colin M.E.ORCID,Cao Sha,Perkins Susan M.,Francomano Clair A.

Funder

National Human Genome Research Institute

National Institutes of Health

Publisher

Elsevier BV

Reference46 articles.

1. Hypermobile Ehlers-Danlos syndromes: complex phenotypes, challenging diagnoses, and poorly understood causes;Gensemer;Dev Dyn,2021

2. Neurological manifestations of Ehlers-Danlos syndrome(s): a review;Castori;Iran J Neurol,2014

3. Ehlers-Danlos syndrome: how to diagnose and when to perform genetic tests;Sobey;Arch Dis Child,2015

4. Ehlers Danlos syndrome and gastrointestinal manifestations: a 20-year experience at Mayo Clinic;Nelson;Neurogastroenterol Motil,2015

5. Survey of the delay in diagnosis for 8 rare diseases in Europe (EURORDISCARE 2). EURODIS. Accessed March 30, 2022. https://www.myobase.org/index.php?lvl=notice_display&id=19890&lang_sel=en_UK

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