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progéria
SYS d011371 LBL 00000nx--j22000003--45-- 005 20240119201139.6 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a progéria $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 330 1-
$a An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA. $8 eng 450 $a Hutchinson-Gilford Syndrome $5 e $8 eng 450 $a Hutchinsonov-Gilfordov syndróm $5 e $8 slo 450 $a nanizmus senilný $5 e $8 slo 550 $3 sllk_un_auth*d003057 $Y Cockayne Syndrome $5 F $a Cockayneov syndróm 550 $3 sllk_un_auth*d014898 $Y Werner Syndrome $5 F $a Wernerov syndróm 686 $a C16.320.488.875 686 $a C16.320.565.753 686 $a C18.452.648.753 750 $a Progeria $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20070706 980 $x M
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