Number of the records: 1
Charcotova-Marieho-Toothova choroba
Record number d002607 Date 04.07.2025 Type M - MESH Topical term Charcotova-Marieho-Toothova choroba Other term English (Pseudonym) Atrophy, Muscular, Peroneal
English (Pseudonym) Hereditary Motor, and Sensory Neuropathy Type I
English (Pseudonym) Hereditary Motor and Sensory-Neuropathy Type II
English (Pseudonym) HMSN Type I
English (Pseudonym) HMSN Type II
English (Pseudonym) Muscular Atrophy, Peroneal
English (Pseudonym) Peroneal Muscular Atrophy
English (Pseudonym) Roussy-Levy Syndrome
English (Pseudonym) Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A
English (Pseudonym) Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1B
English (Pseudonym) Charcot-Marie-Tooth Disease, Demyelinating, Type 1A
English (Pseudonym) Charcot-Marie-Tooth Disease, Demyelinating, Type 1B
English (Pseudonym) Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy
English (Pseudonym) Roussy-Levy Disease
Slovak (Pseudonym) Charcotova-Marieho choroba
Slovak (Pseudonym) atrofia svalová peroneálna
Slovak (Pseudonym) atrofia muskulárna peroneálna
Slovak (Pseudonym) neuropatia hereditárna motoricko-senzitívna
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ I
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ II
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, autozomálne dominantná, s fokálne zloženými myelínovými pošvami, typ 1A
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, autozomálne dominantná, s fokálne zloženými myelínovými pošvami, typ 1B
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, demyelinizačná, typ 1A
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, demyelinizačná, typ 1B
Slovak (Pseudonym) Charcot-Marie-Toothova choroba s typom pomalého nervového vedenia, spojená s lokusom Duffy
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, typ 1A
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, typ 1B
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, typ I
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, typ IA
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, typ IB
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, typ II
Slovak (Pseudonym) HMSN distálna,typ I
Slovak (Pseudonym) neuropatia distálna hereditárna motorická, typ I
Slovak (Pseudonym) HMSN, typ I
Slovak (Pseudonym) HMSN, typ II
Slovak (Pseudonym) HMSN 1A
Slovak (Pseudonym) HMSN 1B
Slovak (Pseudonym) HMSN I
Slovak (Pseudonym) HMSN IA
Slovak (Pseudonym) HMSN IB
Slovak (Pseudonym) HMSN II
Slovak (Pseudonym) HMSN1A
Slovak (Pseudonym) HMSN1B
Slovak (Pseudonym) dedičná areflexická dystázia
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ IB
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ 1A
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ 1B
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ IA
Slovak (Pseudonym) atrofia peroneálnych svalov
Slovak (Pseudonym) atrofia peroneálna svalová
Slovak (Pseudonym) Roussyho-Lévyho dedičná areflexická dystázia
Slovak (Pseudonym) Roussyho-Lévyho syndróm
Slovak (Pseudonym) CMT choroba
See also (Skutočné meno) proteín myelínový P0
(Later heading) proteín myelínový P0
(Later heading) proteín Egr-2
UDC C10.500.300.200C10.574.500.495.200C10.668.829.800.300.200C16.131.666.300.200C16.320.400.375.200 Note 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) 
subject heading
Number of the records: 1