Počet záznamov: 1
retinoblastóm
SYS d012175 LBL 00000nx--j22000003--45-- 005 20240119201338.8 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a retinoblastóm $x BL $x BS $x CF $x CH $x CI $x CL $x CN $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 SC $x SU $x TH $x UL $x UR $x VE $x VI $8 slo 330 1-
$a A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) $8 eng 450 $a Glioblastoma, Retinal $5 e $8 eng 450 $a Glioma, Retinal $5 e $8 eng 450 $a Neuroblastoma, Retinal $5 e $8 eng 450 $a glioblastóm retiny $5 e $8 slo 450 $a glióm retiny $5 e $8 slo 450 $a glioblastóm sietnice $5 e $8 slo 450 $a glióm sietnice $5 e $8 slo 550 $3 sllk_un_auth*d016161 $Y Genes, Retinoblastoma $5 F $a gény retinoblastómu 550 $3 sllk_un_auth*d016161 $Y Genes, Retinoblastoma $5 B $a gény retinoblastómu 550 $3 sllk_un_auth*d019572 $Y Retinal Neoplasms $5 B $a nádory sietnice 686 $a C04.557.465.625.600.725 686 $a C04.557.470.670.725 686 $a C04.557.580.625.600.725 686 $a C04.588.364.818.760 686 $a C11.270.862 686 $a C11.319.475.760 686 $a C11.768.717.760 750 $a Retinoblastoma $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20000622 820 $a coordinate IM with RETINAL NEOPLASMS (IM); /genetics: consider also GENES, RETINOBLASTOMA $8 eng 980 $x M
Počet záznamov: 1