Table of contents for Management of genetic syndromes / edited by Suzanne B. Cassidy, Judith E. Allanson.


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Foreword to the Second Edition. 
 Foreword to the First Edition. 
 Preface. 
 1. Introduction (Suzanne B. Cassidy and Judith E. Allanson). 
 2. Aarskog Syndrome (Roger E. Stevenson). 
 3. Achrondroplasia (Richard M. Pauli). 
 4. Alagille Syndrome (Binita M. Kamath and Ian Krantz). 
 5. Albinism (Richard A. King and C. Gail Summers). 
 6. Angelman Syndrome (Charles A. Williams). 
 7. Arthrogryposis (Judith G. Hall). 
 8. ATR-X (Richard J. Gibbons). 
 9. Bardet-Biedl Syndrome (Anne M. Slavotinek). 
 10. Beckwith-Wiedemann Syndrome (Rosanna Weksberg and Cheryl Shuman). 
 11. CHARGE Association (Christine A. Oley). 
 12. Coffin-Lowry Syndrome (Alasdair G.W. Hunter). 
 13. Cornelia de Lange Syndrome (David E. Fitzpatrick and Antonie D. Kline). 
 14. Costello Syndrome (Angela E. Lin, Karen W. Gripp and Bronwyn Kerr). 
 15. Craniosynostosis (Karen W. Gripp and ElaineH. Zackai). 
 16. Denys-Drash Syndrome (Carol L. Clericuzio). 
 17. Down Syndrome (Alasdair G.W. Hunter). 
 18. Ehlers-Danlos Syndrome (Richard J. Wenstrup and Leah B. Hoechstetter). 
 19. Fetal Alcohol Syndrome (AlbertE. Chudley and Sally E. Longstaffe). 
 20. Fetal Anticonvulsants (Renata C. Gallagher, Kerry Kingham and H. Eugene Hoyme). 
 21. Fragile X Syndrome (Randi J. Hagerman). 
 22. Gorlin Syndrome (Nevoid Basal Cell Carcinoma Syndrome) (Peter Farndon). 
 23. Hereditary Haemorrhagic Telangiectasia (Mary E.M. Porteous). 
 24. Holoprosencephaly (Andrea L. Gropman and Maximilian Muenke). 
 25. Incontinetia Pigmenti (Dian Donnai). 
 26. Kabuki Syndrome (Louanne Hudgins). 
 27. Klinefelter Syndrome (Joe Leigh Simpson, John M. Graham, Carol Samango-Sprouse and Ronald Swerdloff). 
 28. Marfan Syndrome (Iris Schrijver, Deborah M. Alcorn andUta Francke). 
 29. Myotonic Dystrophy (ChristineE.M. deDie Smulders, Frans G.I. Jennekens and Chris J. Höweler). 
 30. Neurofibromatosis Type 1 (David Viskochil). 
 31. Noonan Syndrome (Judith E. Allanson). 
 32. Oculo-Auriculo-Vertebral Spectrum (Robert J. Gorlin). 
 33. Osteogenesis Imperfecta (Joan C, Marin, Anne Letocha and Edith J. Chernoff). 
 34. Pallister-Hall and Greig Cephalopolysyndactyly Syndrome (Leslie G. Biesecker). 
 35. Prader-Willi Syndrome (Suzanne B. Cassidy). 
 36. Proteus Syndrome (Leslie G. Biesecker). 
 37. Rett Syndrome (Eric E. Smeets and Connie T.R.M. Schrander-Stumpel). 
 38. Robin Sequence (Robert J. Shprintzen). 
 39. Rubinstein-Taybi Syndrome (Raoul C.M. Hennekam). 
 40. Russell-Silver Syndrome (Howard M. Saal). 
 41. Smith-Lemli-Opitz Syndrome (Christopher Cunniff and Theresa A. Grebe). 
 42. Smith-Magenis Syndrome (Ann C.M. Smith). 
 43. Sotos Syndrome (Trevor R.P. Cole). 
 44. Stickler Syndrome (Clair Francomano, Douglas J. Wilkin and Ruth M. Liberfarb). 
 45. Terminal 22q-(Mary C. Phelan, Gail A. Stapleton and R. Curtis Rogers). 
 46. Treacher-Collins Syndrome (Marilyn C. Jones). 
 47. Trisomy 13 and 18 Syndromes (John C. Carey). 
 48. Tuberous Sclerosis (John R.W. Yates). 
 49. Turner Syndrome (Virginia P. Sybert). 
 50. VATER Syndrome (Bryan D. Hall). 
 51. Velo-Cario-Facial Syndrome (Robert J. Shprintzen). 
 52. Von Hippel Lindau Syndrome (R. Neil Schimke and Debra L. Collins). 
 53. WAGR Syndrome (Carol L._ _Clericuzio). 
 54. Williams Syndrome (Colleen A. Morris). 
 55. Wolf-Hirschhorn (Agatino Battaglia). 
 
 


Library of Congress subject headings for this publication: Genetic disorders, Genetic Diseases, Inborn diagnosis, Abnormalities, Multiple diagnosis, Abnormalities, Multiple therapy, Genetic Diseases, Inborn therapy