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Oxford University Press Inc
01 September 1999
Medical genetics; Diseases & disorders; Urology & urogenital medicine
There have been many exciting advances in our understanding of mammalian sex determination and differentiation in the last decade. Using these advances to elucidate clinical conditions of abnormal sexual development, the authors bring together great expertise in molecular endocrinology, molecular genetics, and dysmorphology. The text begins with a discussion of normal gonadal and sexual development that presents enough embryology, biochemistry, and endocrinology to make the remaining chapters easy to assimilate. Then the authors discuss overarching clinical issues that are common to genetic abnormalities of gonadal and sexual development, providing a detailed account of genetic causes of gonadal maldevelopment, followed by a compendium of the singular, syndromal, endocrinologic, and systemic-metabolic genetic causes of sexual maldevelopment. The final section describes genetic forms of gamete failure. Seldom dogmatic, this unconventional textbook frequently presents alternatives, highlights speculation, raises questions, and attempts to provide answers. Yet it will be a uniquely valuable reference on an area of genetic medicine where much has happened in recent years. This book will be welcomed by medical geneticists, genetic counselors, endocrinologists, gynecologists, urologists, and students who need fully-referenced information about the genetic aspects of humans sexual maldevelopment in order to better manage their patients and their patients families.
By:   Leonard Pinsky (Professor and Chair of the Department of Human Genetics Professor and Chair of the Department of Human Genetics McGill University), Robert P. Erickson (Professor of Pediatrics and Genetics, Professor of Pediatrics and Genetics, University of Arizona), R. Neil Schimke (Professor of Medicine and Pediatrics, Professor of Medicine and Pediatrics, University of Kansas), R. Neil Schimke (Professor of Medicine and Pediatrics, University of Kansas, USA)
Imprint:   Oxford University Press Inc
Country of Publication:   United States
Volume:   38
Dimensions:   Height: 264mm,  Width: 186mm,  Spine: 29mm
Weight:   1.234kg
ISBN:   9780195109078
ISBN 10:   0195109074
Series:   Oxford Monographs on Medical Genetics
Pages:   428
Publication Date:   01 September 1999
Audience:   Professional and scholarly ,  Undergraduate
Format:   Hardback
Publisher's Status:   Active

Reviews for Genetic Disorders of Human Sexual Development

This book would make a valuable additiont o the library of any medical school or hospital where there is a clinical genetics or endocrine servoce. It will serve as a good reference source for a range of readers from medical students through clinical geneticists and endocrinologists, and it provides a good mix of practical clinical material and up-to-date biology. --Clinical and Investigative Medicine The authors of Genetic Disorders of Human Social Development recognized the need for an update on the achievements in this area and have provided a very good synopsis. The three authors are a perfect team, since they are recognized experts in pediatrics and genetics....In general, this book is well written, up to date, thorough, and logically organized. It could become the definitive textbook on genetic disorders of human sexual development....a valuable reference that should interest every pediatrician, endocrinologist, urologist, andrologist, gynecologist, and geneticist who deals with disorders of the reproductive system. New England Journal of Medicine The writing is succinct, clear, and well edited. This is a solid readable book that is rich in information. It should be on the shelves for all who care for those with these anomalies, and it should be accessible on library shelves to students of health care and to medical residents. -- Alasdair Hunter, Annals RCPSC, Vol 33, No. 7, Oct 2000 ...a welcome addition to the clinicla genetic pantheon. It fits nicely in the excellent Oxford monograph series (N=38). The authors cover most key topics in this complex field...The books strengths naturally reflect those of its authors- genetic control of sex determination; disorders affecting gonadotropins, steroid biosynthetic pathways and sex hormone receptors; and multiple malformation syndromes. Dysmorphologists should purchase this volume as a resource for 'their' topic alone. Other clinical geneticists and endocrinologists will benefit as well from clinical insight and genetic consideration of rare endocrine disorders. --American Journal of Medical Genetics 2001

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