Charcot-Marie-Tooth Disease [Charcotova-Marieova-Toothova nemoc]
- Terms
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Charcot-Marie-Toothova choroba
Charcotova-Marieova-Toothova nemoc, typ I
Charcotova-Marieova-Toothova nemoc, typ Ia
Charcotova-Marieova-Toothova nemoc, typ Ib
CMT
hereditární motorické a senzitivní neuropatie, typ 1A
hereditární motorické a senzitivní neuropatie, typ 1B
hereditární motorické a senzitivní neuropatie, typ I
hereditární motorické a senzitivní neuropatie, typ II
HMSN typ I
HMSN typ II
syndrom Roussy-Levyové
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Atrophy, Muscular, Peroneal
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
Hereditary Areflexic Dystasia
Hereditary Motor and Sensory Neuropathy 1A
Hereditary Motor and Sensory Neuropathy 1B
Hereditary Motor and Sensory Neuropathy IA
Hereditary Motor And Sensory Neuropathy IB
Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor, and Sensory Neuropathy Type I
Hereditary Type I Motor and Sensory Neuropathy
HMN Distal Type I
HMSN 1A
HMSN 1B
HMSN I
HMSN IA
HMSN IB
HMSN II
HMSN Type I
HMSN Type II
HMSN1A
HMSN1B
Muscular Atrophy, Peroneal
Neuropathy, Type I Hereditary Motor and Sensory
Neuropathy, Type II Hereditary Motor and Sensory
Peroneal Muscular Atrophy
Roussy Levy Hereditary Areflexic Dystasia
Roussy-Levy Disease
Roussy-Levy Hereditary Areflexic Dystasia
Roussy-Levy Syndrome
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)
- DUI
- D002607 MeSH Browser
- CUI
- M0003994
- History note
- 2000(1966)
- Public note
- 2000; see CHARCOT-MARIE DISEASE 1991-1999, see MUSCULAR ATROPHY, SPINAL 1988-1990, see MUSCULAR ATROPHY 1966-1987; for CHARCOT-MARIE-TOOTH DISEASE see CHARCOT-MARIE DISEASE 1991-1999
Allowable subheadings
- BL
- blood 2
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 9
- CO
- complications 10
- DI
- diagnosis 63
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 2
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 2
- EH
- ethnology 4
- ET
- etiology 11
- GE
- genetics 85
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 5
- MI
- microbiology 1
- MO
- mortality 1
- NU
- nursing 1
- PS
- parasitology 0
- PA
- pathology 16
- PP
- physiopathology 15
- PC
- prevention & control 1
- PX
- psychology 3
- RT
- radiotherapy 0
- RH
- rehabilitation 9
- SU
- surgery 5
- TH
- therapy 29
- UR
- urine 0
- VE
- veterinary 0
- VI
- virology 0