Ehlers-Danlos syndrome, classical type (Q46616): Difference between revisions
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Síndrome de Ehlers-Danlos, tipo clássico 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 pelos seguintes critérios diagnósticos clínicos principais: pele hiperextensível, cicatrizes cutâneas atróficas devidas à fragilidade cutânea e hiperfrouxidão articular. | |||
| description / en | description / en | ||
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. | |||
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. |
