Ehlers–Danlos syndrome facts for kids
Ehlers–Danlos syndrome (EDS) is a rare genetic connective tissue disorder. There is no cure. The symptoms include unusually stretchy skin, double-jointedness, flat feet, joint pain, as well as early onset arthritis. More rare and severe forms of the condition also affect the veins (Vascular EDS) and in very rare cases the major organs are affected. There are six main types of EDS. They are:
- Type 3 - Hypermobility
- Types 1 & 2 - Classical
- Type 4 - Vascular
- Type 6 - Kyphoscoliosis
- Types 7A and B - Arthrochalasia
- Type 7C - Dermatosparaxis
Images for kids
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The collagen fibril and EDS: (a) Normal collagen fibrils are of uniform size and spacing. Fibrils from a person with dermatosparaxis (b) show dramatic alterations in fibril morphology with severe effects on the tensile strength of connective tissues. A person with classical EDS (c) shows composite fibrils. Fibrils from a TNX-deficient person (d) are uniform in size and no composite fibrils are seen. TNX-null (e) fibrils are less densely packed and not as well aligned to neighboring fibrils.
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Individual with EDS displaying hypermobile metacarpophalangeal joints
See also
In Spanish: Síndromes de Ehlers-Danlos para niños