Syndromes of the Head and NeckOxford University Press, 27 set 2001 - 1344 pagine This classic text, one of the true anchors of our clinical genetics publishing program, covers over 700 different genetic syndromes involving the head and neck, and it has established itself as the definitive, comprehensive work on the subject. The discussion covers the phenotype spectrum, epidemiology, mode of inheritance, pathogenesis, and clinical profile of each condition, all of which is accompanied by a wealth of illustrations. The authors are recognized leaders in the field, and their vast knowledge and strong clinical judgment will help readers make sense of this complex and burgeoning field. Dr. Gorlin retires as editor in this edition and co-editor Raoul Hennekam takes over. Dr. Hennekam is regarded as one of the top dysmorphologists--and indeed one of the top clinical geneticists--in the world. Judith Allanson is new to the book but is a veteran OUP author and a widely respected geneticist, and Ian Krantz at Penn is a rising star in the field. Dr. Gorlin's name has always been closely associated with the book, and it has now become part of the title. As in all fields of genetics, there has been an explosion in the genetics of dysmorphology syndromes, and the author has undertaken a complete updating of all chapters in light of the discoveries of the Human Genome Project and other ongoing advances, with some chapters requiring complete rewriting. Additional material has been added both in terms of new syndromes and in updating information on existing syndromes. The book will appeal to clinical geneticists, pediatricians, neurologists, head and neck surgeons, otolarynologists, and dentists. The 4th edition, which published in 2001, has sold 2,600 copies. |
Dall'interno del libro
Risultati 1-5 di 82
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... Clin Genet 5 : 173-177 , 1974 . 62. Hadlock FP et al : Sonography of fetal urinary tract anomalies . Am J Radiol 137 : 261-267 , 1981 . 63. Halal F et al : Acrorenal mandibular syndrome . Am J Med Genet 5 : 277–284 , 1980 . 64. Hammar I ...
... Clin Genet 5 : 173-177 , 1974 . 62. Hadlock FP et al : Sonography of fetal urinary tract anomalies . Am J Radiol 137 : 261-267 , 1981 . 63. Halal F et al : Acrorenal mandibular syndrome . Am J Med Genet 5 : 277–284 , 1980 . 64. Hammar I ...
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... Clin Genet 17 : 375–384 , 1980 ; 18 : 6-12 , 1980 . 17. Magill HL et al : 4p- ( Wolf - Hirschhorn ) syndrome . Am J Roentgenol 135 : 283-288 , 1980 . 18. Martsolf JT et al : Familial transmission of Wolf syndrome resulting from specific ...
... Clin Genet 17 : 375–384 , 1980 ; 18 : 6-12 , 1980 . 17. Magill HL et al : 4p- ( Wolf - Hirschhorn ) syndrome . Am J Roentgenol 135 : 283-288 , 1980 . 18. Martsolf JT et al : Familial transmission of Wolf syndrome resulting from specific ...
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... Clin Genet 26:209–215, 1984. 2. Catrinel Marinescu R et al: FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome. Clin Genet 56:282–288, 1999. 2a. Cornish KM et al: Cognitive functioning in children with ...
... Clin Genet 26:209–215, 1984. 2. Catrinel Marinescu R et al: FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome. Clin Genet 56:282–288, 1999. 2a. Cornish KM et al: Cognitive functioning in children with ...
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... Clin Genet 12 : 28-38 , 1977 . 16. Rogers RC et al : Mosaic trisomy 8 associated with jejunal duplication . Clin Genet 40 : 254–255 , 1991 . 17. Silengo MC et al : Radiologic features in trisomy 8. Pediatr Radiol 8 : 116– 118 , 1979 ...
... Clin Genet 12 : 28-38 , 1977 . 16. Rogers RC et al : Mosaic trisomy 8 associated with jejunal duplication . Clin Genet 40 : 254–255 , 1991 . 17. Silengo MC et al : Radiologic features in trisomy 8. Pediatr Radiol 8 : 116– 118 , 1979 ...
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... Genet Hum 25 : 95–107 , 1977 . 7. Cohen MM Jr : Craniosynostosis in Ullrich - Turner syndrome . Am J Med Genet 35 : 289–290 , 1990 . 8. de Grouchy J , Turleau C : Clinical Atlas of Human Chromosomes . John Wiley & Sons , New York , 1977 ...
... Genet Hum 25 : 95–107 , 1977 . 7. Cohen MM Jr : Craniosynostosis in Ullrich - Turner syndrome . Am J Med Genet 35 : 289–290 , 1990 . 8. de Grouchy J , Turleau C : Clinical Atlas of Human Chromosomes . John Wiley & Sons , New York , 1977 ...
Sommario
1 | |
14 | |
35 | |
76 | |
5 Metabolic Disorders | 119 |
The Osteogenesis Imperfectas | 178 |
Chondrodysplasias and Chondrodystrophies | 192 |
Craniotubular Bone Disorders | 281 |
18 Syndromes with Contractures | 765 |
19 Branchial Arch and OralAcral Disorders | 790 |
General Aspects | 850 |
Common and WellKnown Syndromes | 877 |
Other Syndromes | 912 |
Associations | 966 |
WellKnown Syndromes | 977 |
Other Syndromes | 1039 |
Other Skeletal Dysplasias | 305 |
10 Proportionate Short Stature Syndromes | 366 |
11 Overgrowth Syndromes and Postnatal Onset Obesity Syndromes | 399 |
12 Hamartoneoplastic Syndromes | 428 |
13 Syndromes Affecting the Skin and Mucosa | 494 |
General Aspects and WellKnown Syndromes | 654 |
Miscellaneous Syndromes | 671 |
16 Syndromes of Abnormal Craniofacial Contour | 704 |
17 Syndromes Affecting the Central Nervous System | 724 |
26 Syndromes with GingivalPeriodontal Components | 1093 |
27 Syndromes with Unusual Dental Findings | 1107 |
28 WellKnown Miscellaneous Syndromes | 1133 |
29 Other Miscellaneous Syndromes | 1152 |
30 Syndromes of the Eye | 1181 |
Appendix | 1215 |
Index | 1229 |
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Parole e frasi comuni
abnormalities achondroplasia Acta agenesis Ann Genet anomalies Arch arm of chromosome associated autosomal dominant autosomal recessive basal cell carcinoma bilateral Birth Defects Child chondrodysplasia punctata cleft palate Clin Genet clinical Cohen congenital heart cranial Craniofacial cysts deficiency deletion Dermatol described disease disorder distal drome dwarfism embryopathy epiphyses facial facies fetal findings gene Gorlin growth hearing loss Hum Genet hypertelorism hypophosphatasia hypoplasia hypoplastic infants inheritance Kinderheilkd Lange syndrome lesions lethal limb long bones males malformations manifestations Marfan syndrome maternal Med Genet mental retardation metaphyseal microcephaly micrognathia mild molecular mosaicism mucopolysaccharidosis multiple mutations nasal bridge neonatal normal noted occur Ophthalmol osteogenesis imperfecta osteopetrosis palpebral fissures Partial trisomy Pathol patients Pediatr Pediatr Radiol phalanges phenotype philtrum polyposis Prader-Willi syndrome Prenatal diagnosis radiographic renal reported Rubinstein-Taybi syndrome severe short stature sibs skin skull teeth thanatophoric dysplasia tissue translocation trisomy 18 tumor X-linked Zellweger