Charcot-Marie-Tooth disease, type 4F (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. It is a rare form of CMT4 but the few reported families are from diverse ethnic groups: Lebanese Shiite Muslims, Hispanic North Americans, Nor

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maladie de Charcot-Marie-Tooth type 4F

SNOMEDCT-BE (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. It is a rare form of CMT4 but the few reported families are from diverse ethnic groups: Lebanese Shiite Muslims, Hispanic North Americans, Nor / 715801001

SNOMEDCT-BE (disorder) / 715801001

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A genetic non-syndromic congenital malformation of the neurenteric canal, spinal cord and column characterized by progressive neurologic deterioration (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal

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syndrome de la moelle attachée primaire

SNOMEDCT-BE (pain, sensorimotor deficits, abnormal gait, decreased tone or abnormal reflexes), musculoskeletal / 768939009

SNOMEDCT-BE (disorder) / 768939009

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Charcot-Marie-Tooth disease, type 4C (CMT4C) is a demyelinating CMT peripheral sensorimotor polyneuropathy with early-onset scoliosis or kyphoscoliosis. CMT4C is a relatively frequent form of CMT4: it was first described in Algeria but families have

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maladie de Charcot-Marie-Tooth type 4C

SNOMEDCT-BE (CMT4C) is a demyelinating CMT peripheral sensorimotor polyneuropathy with early-onset scoliosis or kyphoscoliosis. CMT4C is a relatively frequent form of CMT4: it was first described in Algeria but families have / 715797002

SNOMEDCT-BE (disorder) / 715797002

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sensorimotor intelligence

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intelligence sensori-motrice

IATE - Health

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sensorimotor polyneuropathy

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polyneuropathie sensitivo-motrice