Počet záznamov: 1
Stargardtova choroba
SYS d000080362 LBL 00000nx^^^2200181-^^45^^ 005 20240119195339.9 100 $a 20200101asloy0103 ba0 152 $b mesh 250 $a Stargardtova 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 2020(2010) $8 eng 330 1-
$a A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases. $8 eng 450 $a Juvenile Macular Degeneration $5 e $8 eng 450 $a Stargardt Disease 1 $5 e $8 eng 450 $a fundus flavimaculatus $5 e $8 slo 450 $a degenerácia makuly juvenilná $5 e $8 slo 450 $a degenerácia makulárna juvenilná $5 e $8 slo 450 $a dystrofia makulárna so škvrnami, typ 1 $5 e $8 slo 450 $a Stargardtova choroba 1 $5 e $8 slo 450 $a Stargardtova makulárna degenerácia $5 e $8 slo 686 $a C11.270.872 686 $a C11.768.585.439.339 686 $a C16.320.290.724 750 $a Stargardt Disease $8 eng 801 -0
$a SK $b BA006 $c 20200216 801 -2
$a SK $b BA006 $c 20200605 980 $x M
Počet záznamov: 1