Ehlers-Danlos Syndrome

A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability.

Also Known As:

Syndrome, Ehlers-Danlos; Ehlers Danlos Disease; Ehlers-Danlos Disease; Danlos Disease, Ehlers; Disease, Ehlers Danlos; Disease, Ehlers-Danlos; Ehlers Danlos Syndrome; Cutis Elastica

Cardiovascular Diseases: 91362
- Vascular Diseases: 15138
  - Hemostatic Disorders: 250
    - Ehlers-Danlos Syndrome: 799
Hemic and Lymphatic Diseases: 6
- Hematologic Diseases: 3366
  - Hemorrhagic Disorders: 702
    - Hemostatic Disorders: 250
      - Ehlers-Danlos Syndrome: 799
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Skin Abnormalities: 159
    - Ehlers-Danlos Syndrome: 799
- Inborn Genetic Diseases: 11939
  - Genetic Skin Diseases: 47
    - Ehlers-Danlos Syndrome: 799
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Skin Abnormalities: 159
    - Ehlers-Danlos Syndrome: 799
  - Genetic Skin Diseases: 47
    - Ehlers-Danlos Syndrome: 799
- Connective Tissue Diseases: 3269
  - Collagen Diseases: 754
    - Ehlers-Danlos Syndrome: 799

Ghalia Al-Thani Selected Research

Ghalia Al-Thani Research Topics

Disease

Drug/Important Bio-Agent (IBA)