Ehlers-Danlos Syndrome, Type IV D000094623

Related MeSH Hierarchy (8)

Diseases [C] » Cardiovascular Diseases [C14] » Vascular Diseases » Aneurysm » Dissection, Blood Vessel » Aortic Dissection » Ehlers-Danlos Syndrome, Type IV

Diseases [C] » Cardiovascular Diseases [C14] » Vascular Diseases » Hemostatic Disorders » Ehlers-Danlos Syndrome » Ehlers-Danlos Syndrome, Type IV

Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Hemorrhagic Disorders » Hemostatic Disorders » Ehlers-Danlos Syndrome » Ehlers-Danlos Syndrome, Type IV

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Connective Tissue Diseases » Collagen Diseases » Ehlers-Danlos Syndrome » Ehlers-Danlos Syndrome, Type IV

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Ehlers-Danlos Syndrome » Ehlers-Danlos Syndrome, Type IV

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Ehlers-Danlos Syndrome » Ehlers-Danlos Syndrome, Type IV

Description

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).   MeSH

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