Ehlers-Danlos syndrome with periventricular heterotopia (Q101875): Difference between revisions
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A síndrome de Ehlers-Danlos (SED) com heterotopia periventricular é uma variante da SED com manifestações consistentes com SED, incluindo hipermobilidade articular, fragilidade da pele e dilatação aórtica e heterotopia periventricular (HP), que é caracterizada por epilepsia focal geralmente começando na segunda década de vida. A inteligência geralmente é normal. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
