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Sturgeho-Weberov syndróm
SYS d013341 LBL 00000nx--j22000003--45-- 005 20240119200015.9 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a Sturgeho-Weberov 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 $8 slo 300 1-
$a 91(75); was see under ANGIOMATOSIS 1975-90; DIMITRI DISEASE was see STURGE-WEBER SYNDROME 1989-93 $8 eng 330 1-
$a A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects. $8 eng 450 $a Neuroretinoangiomatosis $5 e $8 eng 450 $a Phakomatosis, Sturge-Weber $5 e $8 eng 450 $a neuroretinoangiomatóza $5 e $8 slo 450 $a Sturgeho-Weberova fakomatóza $5 e $8 slo 686 $a C04.557.645.375.850 686 $a C10.562.800 686 $a C14.907.077.850 750 $a Sturge-Weber Syndrome $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20010312 980 $x M
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