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Management of Genetic Syndromes 3rd edition [Kõva köide]

(University of Ottawa, Children's Hospital of Eastern Ontario), (University of California at Irvine, Orange, CA)
  • Formaat: Hardback, 984 pages, kõrgus x laius x paksus: 287x224x43 mm, kaal: 2427 g, Photos: 200 B&W, 0 Color; Drawings: 30 B&W, 0 Color; Tables: 0 B&W, 0 Color
  • Ilmumisaeg: 25-May-2010
  • Kirjastus: Wiley-Blackwell
  • ISBN-10: 0470191414
  • ISBN-13: 9780470191415
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  • Formaat: Hardback, 984 pages, kõrgus x laius x paksus: 287x224x43 mm, kaal: 2427 g, Photos: 200 B&W, 0 Color; Drawings: 30 B&W, 0 Color; Tables: 0 B&W, 0 Color
  • Ilmumisaeg: 25-May-2010
  • Kirjastus: Wiley-Blackwell
  • ISBN-10: 0470191414
  • ISBN-13: 9780470191415
Teised raamatud teemal:
The bestselling guide to the medical management of common genetic syndromes now fully revised and expanded A review in the American Journal of Medical Genetics heralded the first edition of Management of Genetic Syndromes as an "unparalleled collection of knowledge." Since publication of the first edition, improvements in the molecular diagnostic testing of genetic conditions have greatly facilitated the identification of affected individuals. This thorough revision of the critically acclaimed bestseller offers original insights into the medical management of sixty common genetic syndromes seen in children and adults, and incorporates new research findings and the latest advances in diagnosis and treatment of these disorders.

Expanded to cover five new syndromes, this comprehensive new edition also features updates of chapters from the previous editions. Each chapter is written by an expert with extensive direct professional experience with that disorder and incorporates thoroughly updated material on new genetic findings, consensus diagnostic criteria, and management strategies. Edited by two of the field's most highly esteemed experts, this landmark volume provides:





A precise reference of the physical manifestations of common genetic syndromes, clearly written for professionals and families



Extensive updates, particularly in sections on diagnostic criteria and diagnostic testing, pathogenesis, and management



A tried-and-tested, user-friendly format, with each chapter including information on incidence, etiology and pathogenesis, diagnostic criteria and testing, and differential diagnosis



Up-to-date and well-written summaries of the manifestations followed by comprehensive management guidelines, with specific advice on evaluation and treatment for each system affected, including references to original studies and reviews



A list of family support organizations and resources for professionals and families





Management of Genetic Syndromes, Third Edition is a premier source to guide family physicians, pediatricians, internists, medical geneticists, and genetic counselors in the clinical evaluation and treatment of syndromes. It is also the reference of choice for ancillary health professionals, educators, and families of affected individuals looking to understand appropriate guidelines for the management of these disorders.

From a review of the first edition:

"An unparalleled collection of knowledge . . . unique, offering a gold mine of information." American Journal of Medical Genetics

Arvustused

Given that this is a book that has a useful place, potentially, in the clinic of any general paediatrician as will show all the wear and tear features of being well turned and well read."  (Human Genetics, 22 March 2011)

Foreword to the Third Edition xi
Foreword to the Second Edition xiii
Foreword to the First Edition xv
Preface xvii
Contributors xix
Introduction
1(8)
Suzanne B. Cassidy
Judith E. Allanson
Aarskog Syndrome
9(8)
Roger E. Stevenson
Achondroplasia
17(22)
Richard M. Pauli
Alagille Syndrome
39(14)
Binita M. Kamath
Ian D. Krantz
Albinism: Ocular and Oculocutaneous Albinism and Hermansky-Pudlak Syndrome
53(16)
Richard A. King
C. Gail Summers
Angelman Syndrome
69(12)
Charles A. Williams
Aditi Dagli
Arthrogryposis
81(16)
Judith G. Hall
ATR-X: α-Thalassemia Mental Retardation-X-Linked
97(14)
Richard J. Gibbons
Bardet-Biedl Syndrome
111(18)
Anne M. Slavotinek
Beckwith-Wiedemann Syndrome and Hemihyperplasia
129(20)
Rosanna Weksberg
Cheryl Shuman
Bruce Beckwith
Cardio-Facio-Cutaneous Syndrome
149(8)
Maria Ines Kavamura
Giovanni Neri
Charge Syndrome
157(12)
Christine A. Oley
Coffin-Lowry Syndrome
169(14)
Alasdair G. W. Hunter
Cohen Syndrome
183(12)
Kate Chandler
Jill Clayton-Smith
Cornelia de Lange Syndrome
195(16)
David R. Fitzpatrick
Antonie D. Kline
Costello Syndrome
211(16)
Bronwyn Kerr
Karen W. Gripp
Angela E. Lin
Craniosynostosis Syndromes
227(12)
Karen W. Gripp
Elaine H. Zackai
Deletion 1p36 Syndrome
239(10)
Agatino Battaglia
Deletion 4p: Wolf-Hirschhorn Syndrome
249(14)
Agatino Battaglia
Deletion 22q11.2 (Velo-Cardio-Facial Syndrome/DiGeorge Syndrome)
263(22)
Donna M. McDonald-McGinn
Taisa Kohut
Elaine H. Zackai
Deletion 22q13 Syndrome: Phelan-McDermid Syndrome
285(14)
Mary C. Phelan
Gail A. Stapleton
R. Curtis Rogers
Denys-Drash and Frasier Syndromes
299(10)
Carol L. Clericuzio
Down Syndrome
309(28)
Alasdair G. W. Hunter
Ehlers-Danlos Syndromes
337(26)
Brad T. Tinkle
Carrie L. Atzinger
Fetal Alcohol Syndrome and Fetal Alcohol Spectrum Disorder
363(18)
Albert E. Chudley
Sally E. Longstaffe
Fetal Anticonvulsant Syndrome
381(16)
H. Eugene Hoyme
Renata C. Gallagher
Kerry Kingham
Fragile X Syndrome and Premutation-Associated Disorders
397(16)
Randi J. Hagerman
Gorlin Syndrome: Nevoid Basal Cell Carcinoma Syndrome
413(16)
Peter Farndon
Hereditary Hemorrhagic Telangiectasia
429(12)
Mary E.M. Porteous
Jonathan N. Berg
Holoprosencephaly
441(20)
Andrea L. Gropman
Maximilian Muenke
Incontinentia Pigmenti
461(8)
Dian Donnai
Kabuki Syndrome
469(10)
Sarah Dugan
Louanne Hudgins
Klinefelter Syndrome
479(16)
Jeannie Visootsak
John M. Graham
Carole Samango-Sprouse
Ronald Swerdloff
Joe Leigh Simpson
Marfan Syndrome
495(22)
Uta Francke
Mowat-Wilson Syndrome
517(12)
David Mowat
Meredith Wilson
Myotonic Dystrophy Type I
529(20)
Christine E. M. de Die-Smulders
Frans G. I. Jennekens
Carin G. Faber
Neurofibromatosis Type I
549(20)
David Viskochil
Noonan Syndrome
569(18)
Judith E. Allanson
Oculo-Auriculo-Vertebral Spectrum
587(10)
Koenraad Devriendt
Lue de Smet
Ingele Casteels
Osteogenesis Imperfecta
597(18)
Joan C. Marini
Pallister-Hall Syndrome and Greig Cephalopolysyndactyly Syndrome
615(10)
Leslie G. Biesecker
Prader-Willi Syndrome
625(26)
Suzanne B. Cassidy
Shawn E. McCandless
Proteus Syndrome
651(10)
Leslie G. Biesecker
PTEN Hamartoma Tumor Syndrome
661(16)
Emily Edelman
Charis Eng
Rett Syndrome
677(16)
Eric E. Smeets
Connie T. R. M. Schrander-Stumpel
Robin Sequence
693(12)
Howard M. Saal
Rubinstein-Taybi Syndrome
705(12)
Raoul C. M. Hennekam
Russell-Silver Syndrome
717(10)
Howard M. Saal
Smith-Lemli-Opitz Syndrome
727(12)
Christopher Cunniff
Smith-Magenis Syndrome
739(30)
Ann C.M. Smith
Andrea Gropman
Sotos Syndrome
769(18)
Trevor R.P. Cole
Stickler Syndrome
787(10)
Clair A. Francomano
Treacher Collins Syndrome and Related Disorders
797(10)
Marilyn C. Jones
Trisomy 18 and Trisomy 13 Syndromes
807(18)
John C. Carey
Tuberous Sclerosis Complex
825(22)
Hope Northrup
Michael J. Gambello
Kit Sing Ait
Mary Kay Koenig
Turner Syndrome
847(24)
Marsha L. Davenport
Vater/Vacterl Association
871(10)
Bryan D. Hall
Von Hippel-Lindau Syndrome
881(16)
R. Neil Schimke
Debra L. Collins
WAGR Syndrome
897(12)
Carol L. Clericuzio
Williams Syndrome
909(16)
Colleen A. Morris
Index 925
Suzanne Cassidy, MD, is Clinical Professor of Pediatrics at University of California, San Francisco and at University of California, Irvine. She is a board-certified Medical Geneticist and Pediatrician who has focused on care of individuals with genetic syndromes throughout her 30-year academic and clinical career. She is devoted to educating medical geneticists, having served on the American Board of Medical Genetics and the founding Residency Review Committee for Medical Genetics, as well as directed genetics training programs in 4 institutions. She served on the board of directors of the American Society of Human Genetics and as a member of the Board of Scientific Counselors of National Center for Human Genome Research at NIH. She has been identified as one of 'America's Top Doctors'. Judith E. Allanson, MD, is Chief of the Department of Genetics, and Professor of Pediatrics at the University of Ottawa.  She is a board-certified Medical Geneticist and Internist with longstanding interests in pattern recognition, syndrome identification and management.