Hypermobile Ehlers-Danlos Syndrome

Hypermobile Ehlers-Danlos Syndrome is the most common form of Ehlers-Danlos Syndrome, primarily characterized by generalized joint hypermobility, chronic pain, and frequent joint dislocations or subluxations. Unlike other forms of EDS, hEDS currently has no known genetic marker, and diagnosis is based on clinical criteria, including family history, hypermobility scoring, and the presence of other connective tissue-related symptoms. Our clinicians can support you in managing hEDS through a combination of physical therapy, pain management, and lifestyle adjustments to improve joint stability and enhance daily functioning.

POSSIBLE SYMPTOMS
Musculoskeletal: Joint hypermobility / Chronic joint pain / Frequent joint dislocations or subluxations / Muscle fatigue and weakness
Neurological: Brain fog / Anxiety / Dizziness (often due to dysautonomia)
Dermatological: Soft or velvety skin / Easy bruising / Mild skin hyperextensibility
Other: Chronic fatigue / Gastrointestinal issues (e.g., bloating, constipation) / Postural Orthostatic Tachycardia Syndrome (POTS)

Synonyms:
hEDS / Ehlers-Danlos Syndrome Type III / Hypermobility Type Ehlers-Danlos Syndrome

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