Charcot-Marie-Tooth disease type 4G (Q104667): Difference between revisions
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A doença de Charcot-Marie-Tooth tipo 4G (CMT4G) é uma polineuropatia periférica sensitivomotora da CMT desmielinizante identificada em ciganos búlgaros, romenos, franceses e espanhóis e que também é conhecida como neuropatia motora e sensorial hereditária-Russe (HMSNR). O início ocorre entre 8 e 16 anos de idade com fraqueza distal dos membros inferiores, seguida por envolvimento distal dos membros superiores com uma idade de início mais variável entre 10 e 43 anos. A perda sensitiva também é uma característica proeminente. | |||
| description / en | description / en | ||
Charcot-Marie-Tooth disease, type 4G (CMT4G) is a demyelinating CMT peripheral sensorimotor polyneuropathy identified in Bulgarian, Romanian, French, and Spanish Gypsies and is also referred to as hereditary motor and sensory neuropathy-Russe (HMSNR). Onset occurs between 8 and 16 years of age with distal lower limb weakness, followed by distal upper limb involvement with a more variable age of onset of between 10 and 43 years. Sensory loss is also a prominent feature. | |||
Revision as of 10:32, 17 August 2026
Charcot-Marie-Tooth disease, type 4G (CMT4G) is a demyelinating CMT peripheral sensorimotor polyneuropathy identified in Bulgarian, Romanian, French, and Spanish Gypsies and is also referred to as hereditary motor and sensory neuropathy-Russe (HMSNR). Onset occurs between 8 and 16 years of age with distal lower limb weakness, followed by distal upper limb involvement with a more variable age of onset of between 10 and 43 years. Sensory loss is also a prominent feature.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_995395080 |
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| English | Charcot-Marie-Tooth disease type 4G |
Charcot-Marie-Tooth disease, type 4G (CMT4G) is a demyelinating CMT peripheral sensorimotor polyneuropathy identified in Bulgarian, Romanian, French, and Spanish Gypsies and is also referred to as hereditary motor and sensory neuropathy-Russe (HMSNR). Onset occurs between 8 and 16 years of age with distal lower limb weakness, followed by distal upper limb involvement with a more variable age of onset of between 10 and 43 years. Sensory loss is also a prominent feature. |
