Ehlers-Danlos syndrome with periventricular heterotopia (Q101875): Difference between revisions
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15 August 2026
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Latest revision as of 18:43, 16 August 2026
Ehlers-Danlos syndrome (EDS) with periventricular heterotopia is a variant of EDS with features consistent with EDS, including joint hypermobility, skin fragility and aortic dilatation and periventricular heterotopia (PH), which is characterised by focal epilepsy usually beginning in the second decade of life. Intelligence is generally normal.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1856995165 |
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| English | Ehlers-Danlos syndrome with periventricular heterotopia |
Ehlers-Danlos syndrome (EDS) with periventricular heterotopia is a variant of EDS with features consistent with EDS, including joint hypermobility, skin fragility and aortic dilatation and periventricular heterotopia (PH), which is characterised by focal epilepsy usually beginning in the second decade of life. Intelligence is generally normal. |
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CID11:ID_1856995165
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dki-india-ID_1856995165
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Concluído
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15 August 2026
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