Number of the records: 1
progéria
SYS d011371 LBL 00000nz--a2200000o--4500 005 20250606214642.6 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C16.320.488.875 065 $a C16.320.565.753 065 $a C18.452.648.753 066 $a 01 $c 03 150 $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 $2 slo 450 $w v $a Hutchinson-Gilford Syndrome $2 eng 450 $w v $a Hutchinsonov-Gilfordov syndróm $2 slo 450 $w v $a nanizmus senilný $2 slo 550 $7 sllk_us_auth*d003057 $Y Cockayne Syndrome $w p $a Cockayneov syndróm 550 $7 sllk_us_auth*d014898 $Y Werner Syndrome $w p $a Wernerov syndróm 680 9-
$i 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. $2 eng 750 -2
$a Progeria $2 eng 980 $x M
Number of the records: 1