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Arnoldova-Chiariho malformácia
SYS d001139 LBL 00000cx--j2200000---45-- 005 20240119201133.5 100 $a 19990101asloy0103----ba0 152 $b mesh 250 $a Arnoldova-Chiariho malformácia $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 2000(1963) $8 eng 330 1-
$a A group of congenital malformations involving the brainstem, cerebellum, upper spinal cord, and surrounding bony structures. Type II is the most common, and features compression of the medulla and cerebellar tonsils into the upper cervical spinal canal and an associated MENINGOMYELOCELE. Type I features similar, but less severe malformations and is without an associated meningomyelocele. Type III has the features of type II with an additional herniation of the entire cerebellum through the bony defect involving the foramen magnum, forming an ENCEPHALOCELE. Type IV is a form a cerebellar hypoplasia. Clinical manifestations of types I-III include TORTICOLLIS; opisthotonus; HEADACHE; VERTIGO; VOCAL CORD PARALYSIS; APNEA; NYSTAGMUS, CONGENITAL; swallowing difficulties; and ATAXIA. (From Menkes, Textbook of Child Neurology, 5th ed, p261; Davis, Textbook of Neuropathology, 2nd ed, pp236-46) $8 eng 450 $a Arnoldov-Chiariho syndróm $5 e $8 slo 450 $a Arnoldova-Chiariho deformita $5 e $8 slo 550 $3 sllk_un_auth*d010985 $Y Platybasia $5 B $a platybázia 686 $a C10.500.680.291 686 $a C16.131.666.680.291 750 $a Arnold-Chiari Malformation $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20001102 820 $a do not confuse with CHIARI'S SYNDROME see BUDD-CHIARI SYNDROME $8 eng 980 $x M
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