X-linked intellectual deficit, South African type (Q96476): Difference between revisions
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Déficit intelectual, ligado ao X, tipo sul-africano é caracterizado por déficit intelectual grave, mutismo apesar de audição aparentemente normal, dismorfismo craniofacial (face longa e estreita, prognatismo), epilepsia de grande mal, oftalmoplegia e atrofia cerebelar. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Intellectual deficit, X-linked, South African type is characterised by severe intellectual deficit, mutism despite apparently normal hearing, craniofacial dysmorphism (long narrow face, prognathism), grand mal epilepsy, ophthalmoplegia, and cerebellar atrophy. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/37828597 / rank | |||||||||||||||
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CID11:ID_37828597 | |||||||||||||||
| Property / CURIE: CID11:ID_37828597 / rank | |||||||||||||||
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dki-india-ID_37828597 | |||||||||||||||
| Property / Canary Token: dki-india-ID_37828597 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 12:29, 16 August 2026
Intellectual deficit, X-linked, South African type is characterised by severe intellectual deficit, mutism despite apparently normal hearing, craniofacial dysmorphism (long narrow face, prognathism), grand mal epilepsy, ophthalmoplegia, and cerebellar atrophy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_37828597 |
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| English | X-linked intellectual deficit, South African type |
Intellectual deficit, X-linked, South African type is characterised by severe intellectual deficit, mutism despite apparently normal hearing, craniofacial dysmorphism (long narrow face, prognathism), grand mal epilepsy, ophthalmoplegia, and cerebellar atrophy. |
Statements
CID11:ID_37828597
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dki-india-ID_37828597
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Concluído
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15 August 2026
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