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
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.