Ehlers-Danlos syndrome, dysfibronectinaemic type (Q101861): Difference between revisions

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A síndrome de Ehlers-Danlos, tipo fibronectinêmico é um tipo de síndrome de Ehlers-Danlos (SED), um grupo heterogêneo de doenças hereditárias do tecido conjuntivo caracterizadas por hipermobilidade articular variável e hiperextensibilidade cutânea e que se distingue pela disfunção plaquetária associada a uma anormalidade da fibronectina.
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Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality.

Revision as of 18:42, 16 August 2026

Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality.
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    Ehlers-Danlos syndrome, dysfibronectinaemic type
    Ehlers-Danlos syndrome, fibronectinemic type is a type of Ehlers-Danlos syndromes (EDS), a heterogeneous group of inherited connective tissue disorders characterised by variable joint hypermobility and cutaneous hyperextensibility and is distinguished by platelet dysfunction associated with a fibronectin abnormality.

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