How To Pronounce Ehlers Danlos

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The condition Ehlers-Danlos is a group of inherited disorders that affect connective tissues. Connective tissues are proteins that support the skin, bones, and organs. People with Ehlers-Danlos have defects in the proteins that make up these tissues. This can cause the tissues to be weaker and more elastic than usual.

The Ehlers-Danlos National Foundation estimates that the disorder affects 1 in 5,000 to 1 in 20,000 people worldwide.

There are six types of Ehlers-Danlos, which are distinguished by their symptoms.

The most common type is Ehlers-Danlos type III, also known as the hypermobility type. People with this type have loose joints, which can lead to joint pain and dislocation. They may also have fragile skin that bruises easily.

Ehlers-Danlos type IV, also known as the vascular type, is the second most common type. It is characterized by thin, fragile skin that tears easily. People with this type are at an increased risk of developing ruptured blood vessels and organs.

Ehlers-Danlos type VI, also known as the kyphoscoliotic type, is the third most common type. It is characterized by a curvature of the spine, loose joints, and fragile skin.

The other types of Ehlers-Danlos are much less common. They include:

Ehlers-Danlos type I, also known as the classic type. It is characterized by soft, elastic skin that bruises easily.

Ehlers-Danlos type II, also known as the periodontal type. It is characterized by fragile skin and gum tissue.

Ehlers-Danlos type V, also known as the arthrochalasia type. It is characterized by loose joints and fragile skin.

There is no cure for Ehlers-Danlos, but symptoms can be managed with medication and physical therapy.







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