Ehlers-Danlos Syndrome, Type IV

Overview

A subtype of Ehlers-Danlos syndrome (EDS) characterized by vascular pathologies, e.g., AORTIC DISSECTION in addition to common EDS findings, e.g., hyperextensible skin and joints, skin fragility and reduced wound healing capability. It is associated with mutations in collagen type III alpha 1 chain gene (COLLAGEN TYPE III).

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Ehlers-Danlos Syndrome, Type IV

Topic type

Condition

Category

Dermatology

MeSH classification

C14.907.055.448.250.256|C14.907.454.240.500|C15.378.463.515.240.500|C16.131.831.428.500|C16.320.850.260.500|C17.300.200.310.500|C17.800.804.428.500|C17.800.827.260.500

Preparing for an appointment about Ehlers-Danlos Syndrome, Type IV

If you are speaking with a healthcare professional about Ehlers-Danlos Syndrome, Type IV, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

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