Charcot-Marie-Tooth disease type 2B1 (Q104251): Difference between revisions
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A doença de Charcot-Marie-Tooth, tipo 2B1 (CMT2B1, também referida como CMT4C1) é uma polineuropatia periférica sensitivomotora de CMT axonal que foi descrita exclusivamente em famílias originárias do noroeste da África, com início na segunda década de vida. O curso e a gravidade da doença são variáveis, mesmo entre membros afetados da mesma família. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy that has been described exclusively in families originating from North-Western Africa, with onset in the second decade of life. The disease course and severity are variable, even between affected members of the same family. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/957134152 / rank | |||||||||||||||
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CID11:ID_957134152 | |||||||||||||||
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dki-india-ID_957134152 | |||||||||||||||
| Property / Canary Token: dki-india-ID_957134152 / rank | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
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Latest revision as of 10:07, 17 August 2026
Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy that has been described exclusively in families originating from North-Western Africa, with onset in the second decade of life. The disease course and severity are variable, even between affected members of the same family.
| Language | Label | Description | Also known as |
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| default for all languages | ID_957134152 |
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| English | Charcot-Marie-Tooth disease type 2B1 |
Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy that has been described exclusively in families originating from North-Western Africa, with onset in the second decade of life. The disease course and severity are variable, even between affected members of the same family. |
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CID11:ID_957134152
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dki-india-ID_957134152
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Concluído
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16 August 2026
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