Charcot-Marie-Tooth disease type 2G (Q104267): Difference between revisions
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A doença de Charcot-Marie-Tooth autossômica dominante tipo 2G (CMT2G) é uma forma de doença de Charcot-Marie-Tooth axonal, uma neuropatia periférica sensitivomotora. A CMT2G [foi descrita apenas em uma família e] tem início associado a desenvolvimento de deformidades nos pés e dificuldades de deambulação entre a 1ª e a 8ª décadas, com intervalo mediano na 2ª. Fraqueza e perda sensitva envolvem primariamente as pernas e os reflexos tendinosos dos tornozelos estão reduzidos. CMT2G tem um curso lentamente progressivo. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Autosomal dominant Charcot-Marie-Tooth disease type 2G (CMT2G) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2G [has only been described in 1 family and] onset is associated to development of foot deformity and walking difficulties between the 1st and the 8th decades, with a median range in the 2nd one. Weakness and sensory loss involve primarily the legs and ankles tendon reflexes are reduced. CMT2G has a slowly progressive course. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1279608482 / rank | |||||||||||||||
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CID11:ID_1279608482 | |||||||||||||||
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dki-india-ID_1279608482 | |||||||||||||||
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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
Autosomal dominant Charcot-Marie-Tooth disease type 2G (CMT2G) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2G [has only been described in 1 family and] onset is associated to development of foot deformity and walking difficulties between the 1st and the 8th decades, with a median range in the 2nd one. Weakness and sensory loss involve primarily the legs and ankles tendon reflexes are reduced. CMT2G has a slowly progressive course.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1279608482 |
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| English | Charcot-Marie-Tooth disease type 2G |
Autosomal dominant Charcot-Marie-Tooth disease type 2G (CMT2G) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2G [has only been described in 1 family and] onset is associated to development of foot deformity and walking difficulties between the 1st and the 8th decades, with a median range in the 2nd one. Weakness and sensory loss involve primarily the legs and ankles tendon reflexes are reduced. CMT2G has a slowly progressive course. |
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CID11:ID_1279608482
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dki-india-ID_1279608482
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Concluído
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16 August 2026
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