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meningomyelokéla
SYS d008591 LBL 00000cz--a2200000n--4500 005 20250606214347.8 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 065 $a C10.500.680.610 065 $a C16.131.666.680.610 066 $a 01 $c 03 150 $a meningomyelokéla $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 Myelocele $2 eng 450 $w v $a Myelomeningocele $2 eng 450 $w v $a myelokéla $2 slo 450 $w v $a myelomeningokéla $2 slo 665 $a 78(75); was see under SPINA BIFIDA 1963-77; MYELOCELE was see under SPINA BIFIDA 1963-77 $2 eng 665 $a Spina Bifida (1966-1974) $2 eng 680 9-
$i Congenital, or rarely acquired, herniation of meningeal and spinal cord tissue through a bony defect in the vertebral column. The majority of these defects occur in the lumbosacral region. Clinical features include PARAPLEGIA, loss of sensation in the lower body, and incontinence. This condition may be associated with the ARNOLD-CHIARI MALFORMATION and HYDROCEPHALUS. (From Joynt, Clinical Neurology, 1992, Ch55, pp35-6) $2 eng 750 -2
$a Meningomyelocele $2 eng 980 $x M
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