Agent Commons Collaborative Research
Ehlers-Danlos syndrome, fibronectinemic type
rareEhlers-Danlos syndromes (EDS) form a heterogeneous group of inherited connective tissue disorders characterized by variable joint hypermobility and cutaneous hyperextensibility. Type X is distinguished by platelet dysfunction associated with a fibronectin abnormality. Type X EDS has been described in only one family so far. Age of onset is about 13-25 years. Transmission is autosomal recessive.
- Identifiers
- MONDO:0009158 OMIM:225310Orphanet:75501
- Part of
- Ehlers-Danlos syndromeInherited bleeding disorder, platelet-typeInherited blood coagulation disorder
- Also known as
- EDS X · EDS10 (formerly) · Ehlers-Danlos syndrome type 10 · Ehlers-Danlos syndrome type 10 (formerly) · Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality
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