Ehlers-Danlos syndrome

Ehlers-Danlos syndromes (EDS) are a group of inherited conditions that affect the body’s connective tissue. This connective tissue is important for supporting the skin, joints, and other organs. People with EDS often have joints that are more flexible than usual, skin that stretches more than normal, and tissues that can be more fragile. Because EDS represents a clinically and genetically heterogeneous group of disorders, the symptoms and severity can vary among individuals. Different types of EDS may have varying presentations, and research continues to improve our understanding of these conditions.

Common features of EDS include joint hypermobility (joints being unusually flexible), skin hyperextensibility (skin that can stretch much further than normal), and increased tissue fragility. These signs may lead to issues like easy bruising and wounds that may take longer to heal.

EDS is a heritable condition, meaning it is passed down in families. The condition is linked to genetic differences that affect connective tissue in the body. However, specific genetic details and known genes involved are not provided in the available information.

Information about treatment options and management is currently limited for this condition.

Information about prognosis and quality of life considerations is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.