| Description |
xvii, 695 pages : illustrations ; 29 cm |
| Contents |
Aarskog syndrome / Roger E. Stevenson -- Achondroplasia / Richard M. Pauli -- Alagille syndrome / Binita M. Kamath and Ian Krantz -- Albinism / Richard A. King and C. Gail Summers -- Angelman syndrome / Charles A. Williams -- Arthrogryposis / Judith G. Hall -- ATR-X / Richard J. Gibbons -- Bardet-Biedl syndrome / Anne M. Slavotinek -- Beckwith-Wiedemann syndrome / Rosanna Weksberg and Cheryl Shuman -- CHARGE association / Christine A. Oley -- Coffin-Lowry syndrome / Alasdair G.W. Hunter -- Cornelia de Lange syndrome / David E. Fitzpatrick and Antonie D. Kline -- Costello syndrome / Angela E. Lin, Karen W. Gripp and Bronwyn Kerr -- |
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Craniosynostosis / Karen W. Gripp and Elaine H. Zackai -- Denys-Drash syndrome / Carol L. Clericuzio -- Down syndrome / Alasdair G.W. Hunter -- Ehlers-Danlos syndrome / Richard J. Wenstrup and Leah B. Hoechstetter -- Fetal alcohol syndrome / Albert E. Chudley and Sally E. Longstaffe -- Fetal anticonvulsants / Renata C. Gallagher, Kerry Kingham and H. Eugene Hoyme -- Fragile X syndrome / Randi J. Hagerman -- Gorlin syndrome (nevoid basal cell carcinoma syndrome) / Peter Farndon -- Hereditary haemorrhagic telangiectasia / Mary E.M. Porteous -- Holoprosencephaly / Andrea L. Gropman and Maximilian Muenke -- |
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Incontinetia pigmenti / Dian Donnai -- Kabuki syndrome / Louanne Hudgins -- Klinefelter syndrome / Joe Leigh Simpson ... [et al.] -- Marfan syndrome / Iris Schrijver, Deborah M. Alcorn and Uta Francke -- Myotonic dystrophy / Christine E.M. deDie Smulders, Frans G.I. Jennekens and Chris J. H"weler -- Neurofibromatosis type 1 / David Viskochil -- Noonan syndrome / Judith E. Allanson -- Oculo-auriculo-vertebral spectrum / Robert J. Gorlin -- Osteogenesis imperfecta / Joan C, Marin, Anne Letocha and Edith J. Chernoff -- Pallister-Hall and Greig cephalopolysyndactyly syndrome / Leslie G. Biesecker -- |
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Prader-Willi syndrome / Suzanne B. Cassidy -- Proteus syndrome / Leslie G. Biesecker -- Rett syndrome / Eric E. Smeets and Connie T.R.M. Schrander-Stumpel -- Robin sequence / Robert J. Shprintzen -- Rubinstein-Taybi syndrome / Raoul C.M. Hennekam -- Russell-Silver syndrome / Howard M. Saal -- Smith-Lemli-Opitz syndrome / Christopher Cunniff and Theresa A. Grebe -- Smith-Magenis syndrome / Ann C.M. Smith -- Sotos syndrome / Trevor R.P. Cole -- Stickler syndrome / Clair Francomano, Douglas J. Wilkin and Ruth M. Liberfarb -- |
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Terminal 22q- / Mary C. Phelan, Gail A. Stapleton and R. Curtis Rogers -- Treacher-Collins syndrome / Marilyn C. Jones -- Trisomy 13 and 18 syndromes / John C. Carey -- Tuberous sclerosis / John R.W. Yates -- Turner syndrome / Virginia P. Sybert -- VATER syndrome / Bryan D. Hall -- Velo-Cario-facial syndrome / Robert J. Shprintzen -- Von Hippel Lindau syndrome / R. Neil Schimke and Debra L. Collins -- WAGR syndrome / Carol L. Clericuzio -- Williams syndrome / Colleen A. Morris -- Wolf-Hirschhorn / Agatino Battaglia |
| Summary |
"Management of Genetic Syndromes, Second Edition incorporates all the most recent developments in knowledge about and management of the most common genetic syndromes seen in children and adults. Expanded to cover twenty-five new syndromes, this comprehensive new edition also features thorough updates of chapters from the first edition." "Written to be clear and accessible to medical generalists and specialists, as well as allied health and education professionals and families, Management of Genetic Syndromes, Second Edition provides a unique and up-to-date resource for this rapidly developing field."--BOOK JACKET |
| Bibliography |
Includes bibliographical references and index |
| Subject |
Genetic disorders.
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Genetic Diseases, Inborn -- diagnosis.
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Abnormalities, Multiple -- diagnosis.
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Abnormalities, Multiple -- therapy.
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Genetic Diseases, Inborn -- therapy.
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| Author |
Cassidy, Suzanne B.
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Allanson, Judith E.
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| LC no. |
2004004693 |
| ISBN |
0471308706 cloth alkaline paper |
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