Literature DB >> 1227527

The Kleeblattschädel anomaly.

A P Eaton, A Sommer, M P Sayers.   

Abstract

Two cases with the characteristic features of the Kleeblattschädel anomaly are presented. The precise etiology of this rare syndrome is unknown and no genetic or environmental factors have been identified to date. Within the spectrum of disorders characterized by craniostenosis, the Kleeblattschädel anomaly appears to represent the most severe degree of expression. An early aggressive neurosurgical approach to correct the cranial malformation did not significantly alter the poor prognosis in these two patients.

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Year:  1975        PMID: 1227527

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  4 in total

1.  FGFR-associated craniosynostosis syndromes and gastrointestinal defects.

Authors:  Christine E Hibberd; Sarah Bowdin; Yamini Arudchelvan; Christopher R Forrest; Katherine A Brakora; Ralph S Marcucio; Siew-Ging Gong
Journal:  Am J Med Genet A       Date:  2016-08-02       Impact factor: 2.802

Review 2.  Skull base growth in craniosynostosis.

Authors:  James Tait Goodrich
Journal:  Childs Nerv Syst       Date:  2005-05-20       Impact factor: 1.475

3.  The relationship of cloverleaf skull syndrome to hydrocephalus.

Authors:  Y Shiroyama; H Ito; T Yamashita; S Nakano; Y Kurokawa
Journal:  Childs Nerv Syst       Date:  1991-11       Impact factor: 1.475

4.  Ventricular diverticula with localized dysgenesis of the temporal lobe in cloverleaf skull anomaly.

Authors:  A Hori; R L Friede; G Fischer
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

  4 in total

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