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MERRF syndróm
SYS d017243 LBL 00000cz--a2200000o--4500 005 20250606214844.2 008 920522|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C05.651.460.620.530 065 $a C10.228.140.163.100.545 065 $a C10.228.140.490.375.130.650.700 065 $a C10.228.140.490.493.063.650.700 065 $a C10.668.491.500.500.550 065 $a C16.320.565.189.545 065 $a C18.452.132.100.545 065 $a C18.452.648.189.545 065 $a C18.452.660.560.620.530 066 $a 01 $c 03 150 $a MERRF syndróm $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 Fukuhara Disease $2 eng 450 $w v $a Myoclonic Epilepsy with Ragged Red Fibers $2 eng 450 $w v $a Fukuharova choroba $2 slo 450 $w v $a epilepsia myoklonická s drsnými červenými svalovými vláknami $2 slo 665 $a 1993 $2 eng 665 $a Epilepsy, Myoclonic (1980-1992) $2 eng 665 $a Mitochondria, Muscle (1980-1992) $2 eng 680 9-
$i A mitochondrial encephalomyopathy characterized clinically by a mixed seizure disorder, myoclonus, progressive ataxia, spasticity, and a mild myopathy. Dysarthria, optic atrophy, growth retardation, deafness, and dementia may also occur. This condition tends to present in childhood and to be transmitted via maternal lineage. Muscle biopsies reveal ragged-red fibers and respiratory chain enzymatic defects. (From Adams et al., Principles of Neurology, 6th ed, p986) $2 eng 750 -2
$a MERRF Syndrome $2 eng 980 $x M
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