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Charcotova-Marieho-Toothova choroba

Subject h.	Charcotova-Marieho-Toothova choroba
Subject h.	Charcot-Marie-Tooth Disease
Entry terms	Charcotova-Marieho choroba atrofia svalová peroneálna atrofia muskulárna peroneálna neuropatia hereditárna motoricko-senzitívna neuropatia dedičná motorická a senzorická, typ I neuropatia dedičná motorická a senzorická, typ II HMSN, typ I HMSN, typ II dystrofia svalová peroneálna dystrofia muskulárna peroneálna Roussyho-Lévyho syndróm CMT choroba
English X references	Atrophy, Muscular, Peroneal HMSN Type I HMSN Type II Hereditary Motor and Sensory-Neuropathy Type II Hereditary Motor, and Sensory Neuropathy Type I Muscular Atrophy, Peroneal Peroneal Muscular Atrophy Roussy-Levy Syndrome
Scope note in 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 also reference (FX) in Slovak	proteín myelínový P0
See also reference (FX) in English	Myelin P0 Protein
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Number of the records: 1