Ehlers-Danlos syndrome, dermatosparaxis type (Q101859): Difference between revisions
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A síndrome de Ehlers-Danlos, tipo dermatosparaxia 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 do tecido, que é marcada por tecidos extremamente frágeis, pele hiperextensível e facilidade para apresentar hematomas. A pele facial contém numerosas dobras, como na síndrome da cútis laxa. Hérnias umbilicais ou inguinais também foram descritas. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/445808781 / rank | |||||||||||||||
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CID11:ID_445808781 | |||||||||||||||
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dki-india-ID_445808781 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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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 |
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| default for all languages | ID_445808781 |
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| 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. |
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CID11:ID_445808781
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dki-india-ID_445808781
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Concluído
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15 August 2026
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