Search on: HEREDITARY MOTOR, AND SENSORY NEUROPATHY TYPE I 
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Descriptor English:   Charcot-Marie-Tooth Disease 
Descriptor Spanish:   Enfermedad de Charcot-Marie-Tooth 
Descriptor Portuguese:   Doença de Charcot-Marie-Tooth 
Synonyms English:   Areflexic Dystasia, Hereditary
Areflexic Dystasias, Hereditary
Atrophies, Peroneal Muscular
Atrophy, Muscular, Peroneal
Atrophy, Peroneal Muscular
Charcot Marie Disease
Charcot Marie Tooth Disease
Charcot Marie Tooth Disease, Type 1A
Charcot Marie Tooth Disease, Type 1B
Charcot Marie Tooth Disease, Type I
Charcot Marie Tooth Disease, Type IA
Charcot Marie Tooth Disease, Type IB
Charcot Marie Tooth Disease, Type II
Charcot Marie Tooth Hereditary Neuropathy
Charcot Marie Tooth Neuropathy, Type 1A
Charcot Marie Tooth Neuropathy, Type 1B
Charcot Marie Tooth Syndrome
Charcot-Marie Disease
Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A
Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B
Charcot-Marie-Tooth Disease, Demyelinating, Type 1A
Charcot-Marie-Tooth Disease, Demyelinating, Type 1B
Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy
Charcot-Marie-Tooth Disease, Type 1A
Charcot-Marie-Tooth Disease, Type 1B
Charcot-Marie-Tooth Disease, Type I
Charcot-Marie-Tooth Disease, Type IA
Charcot-Marie-Tooth Disease, Type IB
Charcot-Marie-Tooth Disease, Type II
Charcot-Marie-Tooth Hereditary Neuropathy
Charcot-Marie-Tooth Neuropathy, Type 1A
Charcot-Marie-Tooth Neuropathy, Type 1B
Charcot-Marie-Tooth Syndrome
Dystasia, Hereditary Areflexic
Dystasias, Hereditary Areflexic
HMN Distal Type I
HMSN 1A
HMSN 1B
HMSN I
HMSN IA
HMSN IB
HMSN II
HMSN Type I
HMSN Type II
HMSN1A
HMSN1B
Hereditary Areflexic Dystasia
Hereditary Areflexic Dystasias
Hereditary Motor And Sensory Neuropathy IB
Hereditary Motor and Sensory Neuropathy 1A
Hereditary Motor and Sensory Neuropathy 1B
Hereditary Motor and Sensory Neuropathy IA
Hereditary Motor and Sensory Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor, and Sensory Neuropathy Type I
Hereditary Neuropathy, Charcot-Marie-Tooth
Hereditary Type I Motor and Sensory Neuropathy
Muscular Atrophies, Peroneal
Muscular Atrophy, Peroneal
Neuropathy, Type I Hereditary Motor and Sensory
Neuropathy, Type II Hereditary Motor and Sensory
Peroneal Muscular Atrophies
Peroneal Muscular Atrophy
Roussy Levy Disease
Roussy Levy Hereditary Areflexic Dystasia
Roussy Levy Syndrome
Roussy-Levy Disease
Roussy-Levy Hereditary Areflexic Dystasia
Roussy-Levy Syndrome
Syndrome, Charcot-Marie-Tooth
Syndrome, Roussy-Levy  
Tree Number:   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
Definition English:   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) 
See Related English:   Myelin P0 Protein
 
History Note English:   2000(1966) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   24021 
Unique Identifier:   D002607 

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