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de Langeovej syndróm
SYS d003635 LBL 00000nz--a2200000o--4500 005 20250606213908.8 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C10.597.606.360.210 065 $a C16.131.077.272 065 $a C16.131.260.210 065 $a C16.320.180.210 066 $a 01 $c 03 150 $a de Langeovej 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 $2 slo 450 $w v $a Brachmann-De Lange Syndrome $2 eng 450 $w v $a Cornelia De Lange Syndrome $2 eng 450 $w v $a Brachmannov-de Langeovej syndróm $2 slo 450 $w v $a syndróm Cornelie de Langeovej $2 slo 550 $7 sllk_us_auth*d008607 $Y Intellectual Disability $w p $a postihnutie intelektuálne 665 $a 2000(1964) $2 eng 680 9-
$i A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231) $2 eng 750 -2
$a De Lange Syndrome $2 eng 980 $x M
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