Number of the records: 1
Charcotova-Marieho-Toothova choroba
SYS d002607 LBL 00000cz--a2200000n--4500 005 20250704095726.8 008 991108|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 $d BA006 065 $a C10.500.300.200 065 $a C10.574.500.495.200 065 $a C10.668.829.800.300.200 065 $a C16.131.666.300.200 065 $a C16.320.400.375.200 066 $a 01 $c 03 150 $a Charcotova-Marieho-Toothova choroba $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $2 slo 450 $w v $a Atrophy, Muscular, Peroneal $2 eng 450 $w v $a Hereditary Motor, and Sensory Neuropathy Type I $2 eng 450 $w v $a Hereditary Motor and Sensory-Neuropathy Type II $2 eng 450 $w v $a HMSN Type I $2 eng 450 $w v $a HMSN Type II $2 eng 450 $w v $a Muscular Atrophy, Peroneal $2 eng 450 $w v $a Peroneal Muscular Atrophy $2 eng 450 $w v $a Roussy-Levy Syndrome $2 eng 450 $w v $a Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1A $2 eng 450 $w v $a Charcot-Marie-Tooth Disease, Autosomal Dominant, With Focally Folded Myelin Sheaths, Type 1B $2 eng 450 $w v $a Charcot-Marie-Tooth Disease, Demyelinating, Type 1A $2 eng 450 $w v $a Charcot-Marie-Tooth Disease, Demyelinating, Type 1B $2 eng 450 $w v $a Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked To Duffy $2 eng 450 $w v $a Roussy-Levy Disease $2 eng 450 $w v $a Charcotova-Marieho choroba $2 slo 450 $w v $a atrofia svalová peroneálna $2 slo 450 $w v $a atrofia muskulárna peroneálna $2 slo 450 $w v $a neuropatia hereditárna motoricko-senzitívna $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ I $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ II $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, autozomálne dominantná, s fokálne zloženými myelínovými pošvami, typ 1A $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, autozomálne dominantná, s fokálne zloženými myelínovými pošvami, typ 1B $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, demyelinizačná, typ 1A $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, demyelinizačná, typ 1B $2 slo 450 $w v $a Charcot-Marie-Toothova choroba s typom pomalého nervového vedenia, spojená s lokusom Duffy $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, typ 1A $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, typ 1B $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, typ I $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, typ IA $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, typ IB $2 slo 450 $w v $a Charcot-Marie-Toothova choroba, typ II $2 slo 450 $w v $a HMSN distálna,typ I $2 slo 450 $w v $a neuropatia distálna hereditárna motorická, typ I $2 slo 450 $w v $a HMSN, typ I $2 slo 450 $w v $a HMSN, typ II $2 slo 450 $w v $a HMSN 1A $2 slo 450 $w v $a HMSN 1B $2 slo 450 $w v $a HMSN I $2 slo 450 $w v $a HMSN IA $2 slo 450 $w v $a HMSN IB $2 slo 450 $w v $a HMSN II $2 slo 450 $w v $a HMSN1A $2 slo 450 $w v $a HMSN1B $2 slo 450 $w v $a dedičná areflexická dystázia $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ IB $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ 1A $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ 1B $2 slo 450 $w v $a neuropatia dedičná motorická a senzorická, typ IA $2 slo 450 $w v $a atrofia peroneálnych svalov $2 slo 450 $w v $a atrofia peroneálna svalová $2 slo 450 $w v $a Roussyho-Lévyho dedičná areflexická dystázia $2 slo 450 $w v $a Roussyho-Lévyho syndróm $2 slo 450 $w v $a CMT choroba $2 slo 550 $7 sllk_us_auth*d018993 $Y Myelin P0 Protein $w p $a proteín myelínový P0 550 $7 sllk_us_auth*d018993 $Y Myelin P0 Protein $w b $a proteín myelínový P0 550 $7 sllk_us_auth*d051767 $Y Early Growth Response Protein 2 $w b $a proteín Egr-2 665 $a 2000(1966) $2 eng 680 9-
$i 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) $2 eng 750 -2
$a Charcot-Marie-Tooth Disease $2 eng 980 $x M
Number of the records: 1