EDS Zebra Articles

04/08/2026

2026 Returning to Exercise After Valsalva-Induced Carotid Artery Dissection

AbstractBackgroundAlthough standardized clinical guidelines are lacking, structured exercise training (ExT) can safely improve cardiorespiratory fitness and clinical outcomes after internal carotid...

04/08/2026

2026 Spontaneous pneumothorax-associated with genetic disorders

04/07/2026

2026 Spontaneous pneumothorax-associated with genetic disorders

https://journals.sagepub.com/doi/10.1177/17534666261437339

04/07/2026

2026
What Every Vascular Surgeon Should Know About Vascular Ehlers-Danlos Syndrome

04/07/2026

2026 Pulmonary hemorrhage as an early clue: an integrated clinical-imaging-genetic diagnostic insight for vascular Ehlers-Danlos syndrome

Vascular Ehlers-Danlos syndrome (vEDS) is a rare genetic disorder characterized by connective tissue fragility; however, respiratory manifestations such as

04/07/2026

2026 Bi-allelic variants in OLA1 cause a neurodevelopmental disorder with joint hypermobility

Cytoskeletal organization, cell adhesion, and cell motility are key to neuronal development and functional synapses. Obg-like ATPase 1 (OLA1) regulates cell-matrix adhesion by modulating focal adhesion kinase (FAK) levels, therefore regulating cytoskeletal dynamics and cell motility. To date, howeve...

04/06/2026

2026 Craniocervical instability after inadvertent neck hyperextension in Ehlers-Danlos syndrome: a retrospective case series and literature review

Patients with hypermobile Ehlers-Danlos Syndrome (hEDS) are at risk of developing craniocervical instability (CCI). Iatrogenic causes of CCI in hEDS are un

04/06/2026

2026 A rare case of musculocontractural Ehler-Danlos syndrome with cornea plana and juvenile glaucoma

04/06/2026

2026 Oral Manifestations of Non Vascular Ehlers-Danlos Syndrome Cross-Sectional Study

Background Ehlers–Danlos syndromes are rare hereditary connective tissue disorders; however, their oral manifestations remain poorly characterized in molecularly confirmed individuals. The aim of th...

04/06/2026

2026 Vascular Ehlers-Danlos syndrome with ruptured thoracic aortic aneurysm complicated by vascular graft and endograft infection and aortobronchial fistula

The combination of vascular graft or endograft infection and aortic hereditary disease is extremely rare and just as challenging. We report the case of a 40-year-old man presenting with a ruptured saccular aortic isthmus aneurysm treated with ...

04/05/2026

2026 Multi-System Genetic Architecture of Hypermobile Ehlers-Danlos Syndrome: Integrating Machine Learning with Subject-Level Genomic Analysis

Background/Objectives: Hypermobile Ehlers–Danlos syndrome (hEDS) remains genetically unexplained despite decades of clinical investigation, with the molecular basis undefined for the vast majority of cases. This study employs integrated machine learning approaches with rigorous subject-level stati...

04/05/2026

2026 Prevalence of Intracranial and Cervical Artery Abnormalities in Patients with Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders Presenting to an Academic Headache Clinic

Background/Objective: It remains unknown whether patients with the more common forms of hypermobility carry an elevated risk for the development of intracranial/cervical artery abnormalities. The objective of this study was to determine the prevalence of unruptured intracranial aneurysms, spontaneou...