Charcot-Marie-Tooth Disease
A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)
推出的年份: 2000(1966)
树号: C10.500.300.200, C10.574.500.495.200, C10.668.829.800.300.200, C16.131.666.300.200, C16.320.400.375.200
MeSH 单一 ID: D002607
进入的组:
Charcot Marie Tooth Disease
Muscular Atrophy, Peroneal
Atrophies, Peroneal Muscular
Atrophy, Peroneal Muscular
Muscular Atrophies, Peroneal
Peroneal Muscular Atrophies
Peroneal Muscular Atrophy
Charcot-Marie-Tooth Hereditary Neuropathy
Charcot Marie Tooth Hereditary Neuropathy
Hereditary Neuropathy, Charcot-Marie-Tooth
Atrophy, Muscular, Peroneal
Charcot-Marie Disease
Charcot Marie Disease
Charcot-Marie-Tooth Syndrome
Charcot Marie Tooth Syndrome
Syndrome, Charcot-Marie-Tooth
Roussy-Levy Syndrome
Roussy Levy Syndrome
Syndrome, Roussy-Levy
Roussy-Levy Hereditary Areflexic Dystasia
Roussy-Levy Disease
Roussy Levy Disease
Hereditary Areflexic Dystasia
Areflexic Dystasia, Hereditary
Areflexic Dystasias, Hereditary
Dystasia, Hereditary Areflexic
Dystasias, Hereditary Areflexic
Hereditary Areflexic Dystasias
Roussy Levy Hereditary Areflexic Dystasia
Hereditary Type I Motor and Sensory Neuropathy
Hereditary Motor, and Sensory Neuropathy Type I
Neuropathy, Type I Hereditary Motor and Sensory
HMSN I
HMSN Type I
Charcot-Marie-Tooth Disease, Type I
Charcot Marie Tooth Disease, Type I
HMN Distal Type I
HMSN Type II
Neuropathy, Type II Hereditary Motor and Sensory
HMSN II
Charcot-Marie-Tooth Disease, Type II
Charcot Marie Tooth Disease, Type II
Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory Neuropathy Type II
Charcot-Marie-Tooth Disease, Type IA
Charcot Marie Tooth Disease, Type IA
Charcot-Marie-Tooth Disease, Demyelinating, Type 1A
Charcot-Marie-Tooth Disease, Type 1A
Charcot Marie Tooth Disease, Type 1A
HMSN1A
Hereditary Motor and Sensory Neuropathy 1A
Hereditary Motor and Sensory Neuropathy IA
HMSN 1A
HMSN IA
Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A
Charcot-Marie-Tooth Neuropathy, Type 1A
Charcot Marie Tooth Neuropathy, Type 1A
Charcot-Marie-Tooth Disease, Type IB
Charcot Marie Tooth Disease, Type IB
Charcot-Marie-Tooth Disease, Demyelinating, Type 1B
Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy
Charcot-Marie-Tooth Disease, Type 1B
Charcot Marie Tooth Disease, Type 1B
HMSN1B
Hereditary Motor and Sensory Neuropathy 1B
Hereditary Motor And Sensory Neuropathy IB
HMSN 1B
HMSN IB
Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B
Charcot-Marie-Tooth Neuropathy, Type 1B
Charcot Marie Tooth Neuropathy, Type 1B
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