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Craniosynostoses: Molecular Genetics, Principles of Diagnosis, and Treatment (Monographs in Human Genetics), 1E (2011) [PDF][UnitedVRG]

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  Craniosynostoses: Molecular Genetics,
Principles of Diagnosis, and Treatment (Monographs in Human Genetics), 1E
  
  by Maximilian Muenke (Editor), Wolfram Kress (Editor), Hartmut Collmann (Editor), Benjamin D.
Solomon (Editor) 
  
  True PDF,
Bookmarked and Indexed
  
  
  
  ISBN-13: 978-3805595940 | ISBN-10: 3805595948 | Edition: 1 st | March
7, 2011
  
  Craniosynostosis - the premature fusion of the cranial sutures of an infant's skull -
is a challenging and complex condition that can occur as part of a syndrome or in isolation. In the last two decades
increased knowledge about the structure and function of the human genome has enabled the discovery of the molecular
etiologies of most forms of syndromic craniosynostosis, which in turn has allowed for the analysis of normal and
abnormal sutural biology from the atomic to the population-based level. In parallel with the increase in basic
biological understanding, advances in clinical diagnosis and treatment have been achieved including improved prenatal
imaging technology and craniofacial surgical techniques as well as condition-specific care in specialized hospitals and
clinical units. This book represents a comprehensive overview on the subject of craniosynostosis. Its 19 excellent
chapters were written by the foremost authorities in the field for a wide range of readers. They cover topics including
a historical review, basic biological and molecular studies, the various common and uncommon syndromes, nonsyndromic
craniosynostoses, genetic testing, prenatal ultrasonography, and recent methods of neurosurgical and maxillofacial
treatment. Both investigators at the bench and clinicians at the operating table will appreciate this timely book which
will be the definitive volume on craniosynostosis for many years to come. 						

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