Počet záznamov: 1
holoprozencefália
SYS d016142 LBL 00000cx--j22000003--45-- 005 20240119200127.5 100 $a 19920424csloy0103----ba0 152 $b mesh 250 $a holoprozencefália $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 91 $8 eng 300 1-
$a Abnormalities, Multiple (1966-1990) $8 eng 300 1-
$a Brain/abnormalities (1966-1990) $8 eng 330 1-
$a Anterior midline brain, cranial, and facial malformations resulting from the failure of the embryonic prosencephalon to undergo segmentation and cleavage. Alobar prosencephaly is the most severe form and features anophthalmia; cyclopia; severe INTELLECTUAL DISABILITY; CLEFT LIP; CLEFT PALATE; SEIZURES; and microcephaly. Semilobar holoprosencepaly is characterized by hypotelorism, microphthalmia, coloboma, nasal malformations, and variable degrees of INTELLECTUAL DISABILITY. Lobar holoprosencephaly is associated with mild (or absent) facial malformations and intellectual abilities that range from mild INTELLECTUAL DISABILITY to normal. Holoprosencephaly is associated with CHROMOSOME ABNORMALITIES. $8 eng 450 $a Alobar Holoprosencephaly $5 e $8 eng 450 $a Arhinencephaly $5 e $8 eng 450 $a Lobar Holoprosencephaly $5 e $8 eng 450 $a Semilobar Holoprosencephaly $5 e $8 eng 450 $a holoprozencefália alobárna $5 e $8 slo 450 $a arinencefália $5 e $8 slo 450 $a syndróm arinencefalický $5 e $8 slo 450 $a holoprozencefália lobárna $5 e $8 slo 450 $a holoprozencefália semilobárna $5 e $8 slo 686 $a C05.660.207.410 686 $a C10.500.034.875 686 $a C16.131.077.410 686 $a C16.131.260.380 686 $a C16.131.621.207.410 686 $a C16.131.666.034.875 686 $a C16.320.180.380 750 $a Holoprosencephaly $8 eng 801 -0
$a US $b DNLM $c 19920424 801 -2
$a SK $b BA006 $c 20010517 980 $x M
Počet záznamov: 1