Ehlers-Danlos syndrome, dermatosparaxis type (Q101859): Difference between revisions

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Latest 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
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.