Ehlers-Danlos syndrome, dysfibronectinaemic type (Q101861): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 18:42, 16 August 2026
Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1014914201 |
||
| English | Ehlers-Danlos syndrome, dysfibronectinaemic type |
Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality. |
Statements
CID11:ID_1014914201
0 references
dki-india-ID_1014914201
0 references
Concluído
0 references
15 August 2026
0 references
