Number of the records: 1
Charcotova-Marieho-Toothova choroba
SYS d002607 LBL 00000cx--j2200000---45-- 005 20240119201446.0 100 $a 19991108asloy0103----ba0 152 $b mesh 250 $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 $8 slo 300 1-
$a 2000(1966) $8 eng 330 1-
$a 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) $8 eng 450 $a Atrophy, Muscular, Peroneal $5 e $8 eng 450 $a HMSN Type I $5 e $8 eng 450 $a HMSN Type II $5 e $8 eng 450 $a Hereditary Motor and Sensory-Neuropathy Type II $5 e $8 eng 450 $a Hereditary Motor, and Sensory Neuropathy Type I $5 e $8 eng 450 $a Muscular Atrophy, Peroneal $5 e $8 eng 450 $a Peroneal Muscular Atrophy $5 e $8 eng 450 $a Roussy-Levy Syndrome $5 e $8 eng 450 $a Charcotova-Marieho choroba $5 e $8 slo 450 $a atrofia svalová peroneálna $5 e $8 slo 450 $a atrofia muskulárna peroneálna $5 e $8 slo 450 $a neuropatia hereditárna motoricko-senzitívna $5 e $8 slo 450 $a neuropatia dedičná motorická a senzorická, typ I $5 e $8 slo 450 $a neuropatia dedičná motorická a senzorická, typ II $5 e $8 slo 450 $a HMSN, typ I $5 e $8 slo 450 $a HMSN, typ II $5 e $8 slo 450 $a dystrofia svalová peroneálna $5 e $8 slo 450 $a dystrofia muskulárna peroneálna $5 e $8 slo 450 $a Roussyho-Lévyho syndróm $5 e $8 slo 450 $a CMT choroba $5 e $8 slo 550 $3 sllk_un_auth*d018993 $Y Myelin P0 Protein $5 F $a proteín myelínový P0 550 $3 sllk_un_auth*d018993 $Y Myelin P0 Protein $5 B $a proteín myelínový P0 550 $3 sllk_un_auth*d051767 $Y Early Growth Response Protein 2 $5 B $a proteín Egr-2 686 $a C10.500.300.200 686 $a C10.574.500.495.200 686 $a C10.668.829.800.300.200 686 $a C16.131.666.300.200 686 $a C16.320.400.375.200 750 $a Charcot-Marie-Tooth Disease $8 eng 801 -0
$a US $b DNLM $c 19991108 801 -2
$a SK $b BA006 $c 20011024 801 -2
$a SK $b BA006 $c 20100422 801 -2
$a SK $b BA006 $c 20150813 980 $x M
Number of the records: 1