Ehlers-Danlos syndrome, dermatosparaxis type (Q101859): Difference between revisions
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Revision as of 18:42, 16 August 2026
Ehlers-Danlos syndrome, dermatosparaxis type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of hereditary connective tissue diseases characterised by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility, and is marked by extremely fragile tissues, hyperextensible skin and easy bruising. Facial skin contains numerous folds, as in the cutis laxa syndrome. Umbilical or inguinal hernias have also been described.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_445808781 |
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| English | Ehlers-Danlos syndrome, dermatosparaxis type |
Ehlers-Danlos syndrome, dermatosparaxis type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of hereditary connective tissue diseases characterised by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility, and is marked by extremely fragile tissues, hyperextensible skin and easy bruising. Facial skin contains numerous folds, as in the cutis laxa syndrome. Umbilical or inguinal hernias have also been described. |
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CID11:ID_445808781
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dki-india-ID_445808781
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