A 32-year-old Caucasian woman had periodic fevers, skin disease, polyarthralgia and hypermobile joints that were consistent with tumor necrosis factor receptor- associated periodic fever syndrome conWrmed with a Wnding of R92Q missense mutation of the TNFRSFA1 gene with Ehlers-Danlos hypermobility type syndrome. They are both autosomal dominant disorders, and their coexistence suggests that they could share some phenotypic features that may require special consideration in management. Conceivably, they could share common gene mutations although no such data are available.
- Ehlers-Danlos syndrome
- Hypermobility syndrome
- Tumor necrosis factor receptor-Associated periodic fever syndrome