Keywords:
Abnormalities, Human.
;
Electronic books.
Description / Table of Contents:
"The definitive work in genetic evaluation of newborns. I cannot recommend it strongly enough." -Judith G. HallAs demand continues to exceed availability when it comes to clinical geneticists, Genetic Consultations in the Newborn offers an essential new resource for practitioners everywhere: a streamlined diagnostic manual that connects subtle symptoms of newborn dysmorphology to their differential diagnosis.
Type of Medium:
Online Resource
Pages:
1 online resource (401 pages)
Edition:
1st ed.
ISBN:
9780199991006
URL:
https://ebookcentral.proquest.com/lib/geomar/detail.action?docID=5628182
DDC:
618.92/01
Language:
English
Note:
Cover -- Genetic Consultations in the Newborn -- Copyright -- Contents -- Preface -- Acknowledgments -- Abbreviations -- Part I -- 1. Hypotonia -- 2. Intrauterine Growth Restriction -- 3. Overgrowth -- 4. Twins -- 5. Non-Immune Hydrops -- 6. Teratogenic Agents -- Part II -- 7. Cardiac Defects -- 8. Heterotaxy -- Part III -- 9. Ear Anomalies -- 10. Eye Anomalies -- 11. Cleft Lip -- 12. Cleft Palate -- 13. Craniosynostoses -- Part IV -- 14. Macrocephaly and Megalencephaly -- 15. Microcephaly -- 16. Cerebellar Anomalies -- 17. Holoprosencephaly -- 18. Hydrocephalus -- 19. Neural Tube Defects -- 20. Perinatal Arterial Stroke -- Part V -- 21. Diaphragmatic Hernia -- 22. Gastroschisis -- 23. Omphalocele -- 24. Anorectal Malformations -- 25. Hirschsprung Disease -- Part VI -- 26. Renal and Urinary Tract Anomalies -- 27. Hypospadias -- Part VII -- 28. Arthrogryposis -- 29. Clubfoot -- 30. Upper Extremity Anomalies -- 31. Lower Extremity Anomalies -- 32. Polydactyly -- 33. Syndactyly -- Part VIII -- 34. Skeletal Dysplasias: Overview -- 35. Skeletal Dysplasias: Life-Limiting -- 36. Skeletal Dysplasias: Viable -- 37. Skeletal Dysplasias: Fractures in Infancy -- Part IX -- 38. Skin: Ectodermal Dysplasias -- 39. Skin: Epidermolysis Bullosa -- 40. Skin: Ichthyoses -- 41. Skin: Vascular Malformations -- 42. Skin: Other Disorders -- Appendix: Syndromes That Commonly Present in the Newborn -- 1S. Trisomy 21 -- 2S. Trisomy 18 -- 3S. Trisomy 13 -- 4S. Turner Syndrome -- 5S. Wolf-Hirschhorn Syndrome -- 6S. Chromosome 5p Deletion Syndrome -- 7S. Chromosome 22q11.2 Deletion Syndrome -- 8S. Achondroplasia -- 9S. Beckwith-Wiedemann Syndrome -- 10S. CHARGE Syndrome -- 11S. Cornelia de Lange Syndrome -- 12S. Diabetic Embryopathy -- 13S. Fetal Alcohol Spectrum Disorder -- 14S. Incontinentia Pigmenti -- 15S. Prader-Willi Syndrome.
,
16S. Noonan Syndrome and Related Disorders -- 17S. Smith-Lemli-Opitz Syndrome -- 18S. VATER/VACTERL Association -- 19S. Williams Syndrome -- Index.
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