Ehlers-Danlos syndrome, vascular type (Q86807): Difference between revisions

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A síndrome de Ehlers-Danlos tipo IV, também conhecida como o tipo vascular da síndrome de Ehlers-Danlos (EDS), é um transtorno hereditário do tecido conjuntivo definido por manifestações faciais características (acrogéria) na maioria dos pacientes, pele translúcida com vasos subcutâneos altamente visíveis em tronco e parte inferior das costas, facilidade para apresentar hematomas e complicações arteriais, digestivas e uterinas graves, que raramente, ou nunca, são observadas nas outras formas de SED.
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Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.

Revision as of 12:21, 15 August 2026

Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.
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    Ehlers-Danlos syndrome, vascular type
    Ehlers-Danlos syndrome type IV, also known as the vascular type of Ehlers-Danlos syndrome (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial, digestive and uterine complications, which are rarely, if at all, observed in the other forms of EDS.

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