Princeton University Library Catalog

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

Format:
Book
Language:
English
Published/​Created:
Hoboken, N.J. : Wiley-Blackwell, c2010.
Εdition:
3rd ed.
Description:
xxii, 962 p. : ill. ; 29 cm.
Summary note:
"It is imperative for primary care providers and genetic practitioners to have access to appropriate management guidelines for the diagnosis, genetic counseling and management of individuals of all ages affected by relatively common genetic syndromes. This revision of the critically acclaimed bestseller offers original insights into the medical management of 60 syndromes commonly seen by physicians. This fully revised and expanded Third Edition provides family physicians, internists, specialty physicians, medical geneticists, genetic counselors, and families of patients with a more precise reference for study of physical manuifestations of certain syndromes"--Provided by publisher.
Bibliographic references:
Includes bibliographical references and index.
Contents:
1. Introduction / Suzanne B. Cassidy and Judith E. Allanson -- 2. Aarskog Syndrome / Roger E. Stevenson -- 3. Achondroplasia / Richard M. Pauli -- 4. Alagille Syndrome / Binita M. Kamath and Ian D. Krantz -- 5. Albinism: Ocular and Oculocutaneous Albinism and Hermansky-Pudlak Syndrome / Richard A. King and C. Gail Summers -- 6. Angelman Syndrome / Charles A. Williams and Aditi Dagli -- 7. Arthrogryposis / Judith G. Hall -- 8. ATR-X: [alpha]-Thalassemia Mental Retardation-X-Linked / Richard J. Gibbons -- 9. Bardet-Biedl Syndrome / Anne M. Slavotinek -- 10. Beckwith-Wiedemann Syndrome and Hemihyperplasia / Rosanna Weksberg, Cheryl Shuman and Bruce Beckwith -- 11. Cardio-Facio-Cutaneous Syndrome / Maria Ines Kavamura and Giovanni Neri -- 12. CHARGE Syndrome / Christine A. Oley -- 13. Coffin-Lowry Syndrome / Alasdair G. W. Hunter -- 14. Cohen Syndrome / Kate Chandler and Jill Clayton-Smith -- 15. Cornelia de Lange Syndrome / David R. Fitzpatrick and Antonie D. Kline -- 16. Costello Syndrome / Bronwyn Kerr, Karen W. Gripp and Angela E. Lin -- 17. Craniosynostosis Syndromes / Karen W. Gripp and Elaine H. Zackai -- 18. Deletion 1p36 Syndrome / Agatino Battaglia -- 19. Deletion 4p:Wolf-Hirschhorn Syndrome / Agatino Battaglia -- 20. Deletion 22q11.2 (Velo-Cardio-Facial Syndrome/DiGeorge Syndrome) / Donna M. McDonald-McGinn, Taisa Kohut and Elaine H. Zackai -- 21. Deletion 22ql3 Syndrome: Phelan-McDermid Syndrome / Mary C. Phelan, Gail A. Stapleton and R. Curtis Rogers -- 22. Denys-Drash and Frasier Syndromes / Carol L. Clericuzio -- 23. Down Syndrome / Alasdair G. W. Hunter -- 24. Ehlers-Danlos Syndromes / Brad T. Tinkle and Carrie L. Atzinger -- 25. Fetal Alcohol Syndrome and Fetal Alcohol Spectrum Disorder / Albert E. Chudley and Sally E. Longstaffe -- 26. Fetal Anticonvulsant Syndrome / H. Eugene Hoyme, Renata C. Gallagher and Kerry Kingham -- 27. Fragile X Syndrome and Premutation-Associated Disorders / Randi J. Hagerman -- 28. Gorlin Syndrome: Nevoid Basal Cell Carcinoma Syndrome / Peter Farndon -- 29. Hereditary Hemorrhagic Telangiectasia / Mary E. M. Porteous and Jonathan N. Berg -- 30. Holoprosencephaly / Andrea L. Gropman and Maximilian Muenke -- 31. Incontinentia Pigmenti / Dian Donnai -- 32. Kabuki Syndrome / Sarah Dugan and Louanne Hudgins -- 33. Klinefelter Syndrome / Jeannie Visootsak, John M. Graham, Carole Samango-Sprouse, Ronald Swerdloff and Joe Leigh Simpson -- 34. Marfan Syndrome / Uta Francke -- 35. Mowat-Wilson Syndrome / David Mowat and Meredith Wilson -- 36. Myotonic Dystrophy Type 1 / Christine E. M. de Die-Smulders, Frans G. I. Jennekens and Carin G. Faber -- 37. Neurofibromatosis Type 1 / David Viskochil -- 38. Noonan Syndrome / Judith E. Allanson -- 39. Oculo-Auriculo-Vertebral Spectrum / Koenraad Devriendt, Luc de Smet and Ingele Casteels -- 40. Osteogenesis Imperfecta / Joan C. Marini -- 41. Pallister-Hall Syndrome and Greig Cephalopolysyndactyly Syndrome / Leslie G. Biesecker -- 42. Prader-Willi Syndrome / Suzanne B. Cassidy and Shawn E. McCandless -- 43. Proteus Syndrome / Leslie G. Biesecker -- 44. PTEN Hamartoma Tumor Syndrome / Emily Edelman and Charis Eng -- 45. Rett Syndrome / Eric E. Smeets and Connie T. R. M. Schrander-Stumpel -- 46. Robin Sequence / Howard M. Saal -- 47. Rubinstein-Taybi Syndrome / Raoul C. M. Hennekam -- 48. Russell-Silver Syndrome / Howard M. Saal -- 49. Smith-Lemli-Opitz Syndrome / Christopher Cunniff -- 50. Smith-Magenis Syndrome / Ann C. M. Smith and Andrea Gropman -- 51. Sotos Syndrome / Trevor R. P. Cole -- 52. Stickler Syndrome / Clair A. Francomano -- 53. Treacher Collins Syndrome and Related Disorders / Marilyn C. Jones -- 54. Trisomy 18 and Trisomy 13 Syndromes / John C. Carey -- 55. Tuberous Sclerosis Complex / Hope Northrup, Michael J. Gambello, Kit Sing Au and Mary Kay Koenig -- 56. Turner Syndrome / Marsha L. Davenport -- 57. Vater/Vacterl Association / Bryan D. Hall -- 58. von Hippel-Lindau Syndrome / R. Neil Schimke and Debra L. Collins -- 59. WAGR Syndrome / Carol L. Clericuzio -- 60. Williams Syndrome / Colleen A. Morris.
Subject(s):
Genetic disorders [Browse]
ISBN:
  • 9780470191415 (cloth)
  • 0470191414 (cloth)
LCCN:
2009031379
OCLC:
429588902
Related name:
RCP:
C - S