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Reviews
‘[…] the book covers both the clinical aspects and the molecular ones in a very comprehensive way. It is therefore easy to recommend this monograph to professionals in different fields of medicine as well as molecular genetics.’’
Acta Paediatrica Vol. 100, No. 1 (2011)
‘This volume of Monographs in Human Genetics is a welcome addition to the series. Martin Zenker has invited experts within this clinical and molecular field to contribute chapters, including a History of Noonan syndrome and related disorders by Dr. Noonan herself. The format of each chapter follows a pattern which allows each chapter to be read independently and provides a well referenced review of the current knowledge. This does lead to some repetition if one is reading the volume as a whole but that is not a significant criticism.
Each of the clinical chapters is a well written review of the clinical features and related complications of the relevant disorder with good clinical images and illustrations
..The chapters related to the molecular genetics of each condition are well organized and emphasize the contribution of each gene within the overall signaling cascade
This volume is a timely addition to the literature and provides a welcome review of the dysregulation of the Ras-MAPK pathway in Noonan syndrome and the related syndromes. It is very easy to navigate with clear chapters and references. I can certainly recommend it to anyone who wishes to update themselves on this fascinating, evolving story.’
Sally J. Davies
(Human Genetics, Vol. 125, No. 5–6, 2009)
From basic molecular research to clinical practice
In this book, internationally recognized experts review the most important advances regarding the group of human developmental disorders caused by constitutive dysregulation of the Ras-MAPK signalling pathway, including Noonan, cardiofaciocutaneous, LEOPARD and Costello syndromes. A historical overview given by Jacqueline Noonan is followed by chapters dedicated to comprehensive clinical summaries of each condition and up-to-date reviews on associated gene mutations and molecular pathomechanisms. Genotypephenotype correlations are outlined. Further topics include the characterization and underlying mechanisms of common abnormalities in these syndromes such as growth failure, heart defects, and tumor risk. Animal models and the relation to neurofibromatosis type 1 are discussed. The final chapter covers the critical area of treatment including prospects emerging from an improved understanding of the pathophysiology of these disorders.
Providing a concise overview of a very rapidly developing field and suggesting ways how to integrate the latest findings from basic molecular research into clinical practice, this book will be of interest to clinical geneticists, pediatricians, pediatric cardiologists, and pediatric endocrinologists, as well as to human molecular geneticists and other basic researchers working on the RAS pathway.
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