Ehlers-Danlos syndrome, arthrochalasic type (Q101869): Difference between revisions
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A síndrome de Ehlers-Danlos, tipo artrocalásico é um tipo de síndrome de Ehlers-Danlos (EDS), um grupo heterogêneo de doenças hereditárias do tecido conjuntivo caracterizadas por hiperfrouxidão articular, hiperelasticidade cutânea e fragilidade do tecido, e é marcada por luxação congênita bilateral do quadril, hiperfrouxidão das articulações e luxações parciais recorrentes. Outros sinais incluem pele hiperextensível, tecidos frágeis com cicatrizes atróficas e hipotonia muscular. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/96808187 / rank | |||||||||||||||
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CID11:ID_96808187 | |||||||||||||||
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dki-india-ID_96808187 | |||||||||||||||
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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, 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.
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| default for all languages | ID_96808187 |
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| 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. |
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CID11:ID_96808187
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dki-india-ID_96808187
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Concluído
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15 August 2026
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