Ehlers-Danlos syndrome, X-linked (Q101840): Difference between revisions
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Síndrome de Ehlers-Danlos tipo 5 é um tipo de síndrome de Ehlers-Danlos (SED), um grupo heterogêneo de doenças hereditárias do tecido conjuntivo caracterizadas por hiperfrouxidão articular, hiperelasticidade cutânea e fragilidade tecidual, e é caracterizada por pele hiperextensível, mas a fragilidade tecidual e a hiperfrouxidão articular são leves. | |||
| description / en | description / en | ||
Ehlers-Danlos syndrome type 5 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 hyperextensible skin but tissue fragility and joint hyperlaxity are mild. | |||
Revision as of 18:41, 16 August 2026
Ehlers-Danlos syndrome type 5 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 hyperextensible skin but tissue fragility and joint hyperlaxity are mild.
| Language | Label | Description | Also known as |
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| default for all languages | ID_811572965 |
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| English | Ehlers-Danlos syndrome, X-linked |
Ehlers-Danlos syndrome type 5 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 hyperextensible skin but tissue fragility and joint hyperlaxity are mild. |
