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  • 1
    ISSN: 1432-1920
    Keywords: Down's syndrome ; CT scanning ; morphometric change ; basal ganglia calcification ; preniature aging ; small posterior fossa
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We report characteristic and morphometric changes of cranial computed tomography (CT) with increasing age in 56 patients with Down's syndrome aged from 0 month to 37 years. Patients were compared with 142 normal controls aged 0 to 59 years. Width of ventricles, Sylvian fissures, posterior fossa, pons and cisterna magna were measured on CT. The incidences of the cavum septi pellucidi, cavum vergae and cavum veli interpositi and high density in the basal ganglia were examined. There was high incidence (10.7%) of bilateral calcification of basal ganglia in Down's syndrome, although that of pineal body and choroid plexus calcification was similar in Down's syndrome and controls. Basal ganglia calcification is more frequently seen in young Down's syndrome and may be related to the premature aging characteristic of Down's syndrome. The CT in Down's syndrome showed relatively small posterior fossa, small cerebellum, small brain stem and relatively large Sylvian fissures in those under one year of age. There was a high frequency of midline cava and large cisterna magna. There were no significant atrophic changes on CT except after the fifth decade comparing with controls.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-232X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A female infant with distal 15q trisomy and terminal 12q monosomy is reported. This is the first oriental case. Facial dysmorphism in this case is similar to that of previous cases. Additional features are severe brain malformation including Dandy-Walker malformation and agenesis of the corpus callosum, and multiple limb anomalies. These features differed from those of previous cases with the trisomy 15q and may be due to terminal 12q monosomy.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-3432
    Source: Springer Online Journal Archives 1860-2000
    Topics: Psychology
    Notes: Abstract We measured CSF levels of β-endorphin, an opioid hormone, in 19 patients with infantile autism and in 3 patients with Rett syndrome, and compared them with control values. In infantile autism, CSF levels of β-endorphin did not differ significantly from those of age-matched controls. There was no significant correlation between CSF levels and clinical symptoms, including self-injurious behavior, pain insensitivity, and stereotyped movement. However, CSF levels of β-endorphin were significantly higher in the patients with Rett syndrome than in the control (p 〈 .05). Data suggest that neurons containing β-endorphin may not be involved in patients with infantile autism. Thus, there is no relationship between dysfunction of brain opioid and autism.
    Type of Medium: Electronic Resource
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