Ehlers-Danlos syndrome, classical type (Q46616): Difference between revisions
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Revision as of 15:19, 13 August 2026
Ehlers-Danlos syndrome, classic 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 characterised by the following major clinical diagnostic criteria: hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD28.10 |
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| English | Ehlers-Danlos syndrome, classical type |
Ehlers-Danlos syndrome, classic 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 characterised by the following major clinical diagnostic criteria: hyperextensible skin, atrophic cutaneous scars due to tissue fragility and joint hyperlaxity. |
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CID11:LD28.10
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dki-india-LD28.10
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