Počet záznamov: 1
porphyria cutanea tarda
SYS d017119 LBL 00000nx--j22000003--45-- 005 20240119200151.6 100 $a 19920522csloy0103----ba0 152 $b mesh 250 $a porphyria cutanea tarda $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 UR $x VE $x VI $8 slo 300 1-
$a 95; was PORPHYRIA, CUTANEA TARDA 1993-94 $8 eng 300 1-
$a Porphyria (1966-1992) $8 eng 330 1-
$a An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form. $8 eng 686 $a C06.552.830.100 686 $a C16.320.850.742.250 686 $a C17.800.827.742.250 686 $a C18.452.811.400.250 750 $a Porphyria Cutanea Tarda $8 eng 801 -0
$a US $b DNLM $c 19920522 801 -2
$a SK $b BA006 $c 19990910 980 $x M
Počet záznamov: 1