Literature DB >> 1568696

[Neuropsychiatric manifestations of Saethre-Chotzen syndrome].

P Fehlow1, B Fröhlich, W Miosge, W Otto, F Walther.   

Abstract

Four psychiatric patients with SCS are described. All exhibited essential tremor, minimal cerebral dysfunctions, speech disorders, bradyphrenia, disorders of personality with psychasthenie and suspicious traits, restrictions, increased irritability and depressivity, one case of mutism due to abnormal reaction and one of alcohol hallucinosis. The possibility of cosmetic handicap caused by craniofacial dysplasia should be taken into mind and perhaps surgically corrected. Because the craniofacial dysplasia is mostly moderate and the syndactylies are slight the SCS remains often unrecognized, but apart from psychic maldevelopment it is significant as the result of frequent association with other malformations.

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Year:  1992        PMID: 1568696     DOI: 10.1055/s-2007-999125

Source DB:  PubMed          Journal:  Fortschr Neurol Psychiatr        ISSN: 0720-4299            Impact factor:   0.752


  1 in total

1.  Craniosynostosis as a risk factor.

Authors:  P Fehlow
Journal:  Childs Nerv Syst       Date:  1993-09       Impact factor: 1.475

  1 in total

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