Počet záznamov: 1
Laronov syndróm
SYS d046150 LBL 00000nx--j22000003--45-- 005 20240119200458.8 100 $a 20040707csloy0103----ba0 152 $b mesh 250 $a Laronov syndróm $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 2005 $8 eng 300 1-
$a Dwarfism (1976-2004) $8 eng 300 1-
$a Growth Hormone (1976-2004) $8 eng 300 1-
$a Receptors, Cell Surface (1976-2004) $8 eng 300 1-
$a Receptors, Somatotropin (1991-2004) $8 eng 330 1-
$a An autosomal recessive disorder characterized by short stature, defective GROWTH HORMONE RECEPTOR, and failure to generate INSULIN-LIKE GROWTH FACTOR I by GROWTH HORMONE. Laron syndrome is not a form of primary pituitary dwarfism (GROWTH HORMONE DEFICIENCY DWARFISM) but the result of mutation of the human GHR gene on chromosome 5. $8 eng 450 $a Growth Hormone Insensitivity Syndrome $5 e $8 eng 450 $a syndróm necitlivosti na rastový hormón $5 e $8 slo 686 $a C05.116.099.343.679 686 $a C16.320.240.750 686 $a C19.297.656 750 $a Laron Syndrome $8 eng 801 -0
$a US $b DNLM $c 20040707 801 -2
$a SK $b BA006 $c 20050314 980 $x M
Počet záznamov: 1