Ehlers-Danlos syndrome, hypermobility type
Name: |
Ehlers-Danlos syndrome, hypermobility type
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Description: |
Ehlers-Danlos syndrome, hypermobility type (HT-EDS) is the most frequent form of EDS (see this term), a group of hereditary connective tissue diseases, and is characterized by joint hyperlaxity, mild skin hyperextensibility, tissue fragility and extra-musculoskeletal manifestations.
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ORPHAcode: |
285
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Synonyms: |
BJHS
Benign joint hypermobility syndrome
EDS III
Ehlers-Danlos syndrome type 3
Ehlers-Danlos syndrome, hypermobile type
HT-EDS
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
01 May 2019 - 11:58
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