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Gerstmannova-Sträusslerova-Scheinkerova choroba
SYS d016098 LBL 00000cz--a2200000o--4500 005 20250606213956.6 008 920606|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C01.207.800.350 065 $a C10.228.228.800.350 065 $a C10.574.500.425 065 $a C10.574.843.400 065 $a C16.320.400.350 066 $a 01 $c 03 150 $a Gerstmannova-Sträusslerova-Scheinkerova choroba $x BL $x CF $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 SU $x TH $x TM $x UR $x VE $x VI $2 slo 450 $w v $a Gerstmann-Straussler Syndrome $2 eng 450 $w v $a encefalopatia cerebelárna spongiformná chronická $2 slo 450 $w v $a Gerstmannov-Sträusslerov syndróm $2 slo 665 $a 2000(1991); use SLOW VIRUS DISEASES 1988-1990; GERSTMANN-STRAUSSLER-SCHEINKER DISEASE was GERSTMANN-STRAUSSLER-SCHEINDER DISEASE see GERSTMANN-STRAUSSLER SYNDROME 1991 $2 eng 665 $a Slow Virus Diseases (1988-1990) $2 eng 680 9-
$i An autosomal dominant familial prion disease with a wide spectrum of clinical presentations including ATAXIA, spastic paraparesis, extrapyramidal signs, and DEMENTIA. Clinical onset is in the third to sixth decade of life and the mean duration of illness prior to death is five years. Several kindreds with variable clinical and pathologic features have been described. Pathologic features include cerebral prion protein amyloidosis, and spongiform or neurofibrillary degeneration. (From Brain Pathol 1998 Jul;8(3):499-513; Brain Pathol 1995 Jan;5(1):61-75) $2 eng 680 $a a prion dis: do not confuse with GERSTMANN SYNDROME, a type of agnosia $2 eng 750 -2
$a Gerstmann-Straussler-Scheinker Disease $2 eng 980 $x M
Number of the records: 1