Ehlers-Danlos syndrome, arthrochalasic type (Q101869): Difference between revisions
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Latest revision as of 18:42, 16 August 2026
Ehlers-Danlos syndrome, arthrochalasic 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 bilateral congenital hip dislocation, hyperlaxity of the joints, and recurrent partial dislocations. Other signs include hyperextensible skin, fragile tissues with atrophic scars, and muscular hypotonia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_96808187 |
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| English | Ehlers-Danlos syndrome, arthrochalasic type |
Ehlers-Danlos syndrome, arthrochalasic 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 bilateral congenital hip dislocation, hyperlaxity of the joints, and recurrent partial dislocations. Other signs include hyperextensible skin, fragile tissues with atrophic scars, and muscular hypotonia. |
Statements
CID11:ID_96808187
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dki-india-ID_96808187
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Concluído
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15 August 2026
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