Ehlers-Danlos syndrome, vascular type (Q86807): Difference between revisions
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CID11:ID_1202686415 | |||||||||||||||
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dki-india-ID_1202686415 | |||||||||||||||
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13 August 2026
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Latest 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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| default for all languages | ID_1202686415 |
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| English | 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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CID11:ID_1202686415
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dki-india-ID_1202686415
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Concluído
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13 August 2026
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