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Home Fetology

Fetology

Diagnosis and Management of the Fetal Patient

Fergal Malone Mary E. D' Alton Timothy M. Crombleholme Diana W. Bianchi
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  • Fetology - 9780071442015
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Content
The first book to synthesize relevant, critically reviewed data for application to the diagnosis and treatment of prenatal patients? updated and in full color   Fetology: Diagnosis and Management of the Fetal Patient offers a cross-disciplinary approach that goes beyond the traditional boundaries of obstetrics, pediatrics, and surgery to help you effectively diagnose and treat fetal patients. Fetology considers the full implications of a fetal sonographic or chromosomal diagnosis?from prenatal management to long-term outcome?for an affected child. Here, you?ll find all the insights you need to answer the questions of parents faced with a diagnosis of a fetal abnormality?and present them with a coordinated therapeutic plan.   Features * NEW! Full-color design * NEW! Five new chapters on Adrenal Masses, Abdominal Cysts, Overgrowth, Mosaic Trisomy, and DiGeorge Syndrome * NEW! Chapters summarizing contemporary approaches to first and second trimester screening for aneuploidy * NEW! 3D ultrasound and MRI images: over 450 images clearly illustrate the diagnosis of anomalies with the latest, most precise imaging technology * NEW! Key Points open each chapter, providing rapid review of a particular condition * Highlighted treatment/management guidelines deliver quick access to practical, what-to-do information * Each chapter, which covers a single anomaly, includes description of the medical condition, incidence, characteristic sonographic findings, differential diagnosis, best treatment during pregnancy, treatment of the newborn, expected outcome, and more * Addresses gaps in our knowledge that highlight unmet clinical needs and areas for future research Diana W. Bianchi, MD Natalie V. Zucker Professor of Pediatrics, Obstetrics and Gynecology Tufts University School of Medicine Vice Chair for Research and Academic Affairs Department of Pediatrics Floating Hospital for Children at Tufts Medical Center Boston, MA Timothy M. Crombleholme, MD Richard G and Geralyn Azizkhan Chair in Pediatric Surgery Professor of Surgery, Pediatrics (Molecular and Developmental Biology), and Obstetrics and Gynecology University of Cincinnati College of Medicine Associate Director of the Cincinnati Children?s Research Foundation Cincinnati Children?s Hospital Medical Center Cincinnati, OH Mary E. D'Alton, MD Department of Obstetrics and Gynecology Gyn/Division of Maternal-Fetal Medicine Sloane Hospital for Women/New York Presbyterian Hospital New York, NY Fergal D. Malone, MD Professor and Chairman Department of Obstetrics and Gynecology Vice Dean School of Medicine Royal College of Surgeons in Ireland The Rotunda Hospital Dublin, Ireland Table of contents Preface Acknowledgments Part I: Introduction Chapter 1: Prenatal Imaging Chapter 2: First Trimester Screening for Aneuploidy Chapter 3: Second Trimester Screening for Aneuploidy Chapter 4: Prenatal Diagnostic Procedures Chapter 5: Fetal Intervention Part II: Management of Fetal Conditions Diagnosed by Sonography Section A: Central Nervous System Chapter 6: Agenesis of the Corpus Callosum Chapter 7: Anencephaly Chapter 8: Arachnoid Cysts Chapter 9: Cerebral Calcifications Chapter 10: Craniosynostosis Chapter 11: Dandy-Walker Malformation and Variants Chapter 12: Encephalocele Chapter 13: Exencephaly/Acrania Chapter 14: Holoprosencephaly Chapter 15: Hydranencephaly Chapter 16: Hydrocephalus Chapter 17: Intracranial Hemorrhage Chapter 18: Macrocephaly Chapter 19: Myeningomyelocele Chapter 20: Microcephaly Chapter 21: Porencephaly Chapter 22: Vein of Galen Aneurysm Section B: Craniofacial Chapter 23: Cleft Lip and Cleft Palate Chapter 24: Hemifacial Microsomia Chapter 25: Hypertelorism Chapter 26: Hypotelorism Chapter 27: Macroglossia Chapter 28: Micrognathia and Agnathia Chapter 29: Microphthalmia/Anophthalmia Section C: Neck Chapter 30: Congenital High Airway Obstruction Syndrome Chapter 31: Cystic Hygroma in Early Pregnancy Chapter 32: Cystic Hygroma in Late Pregnancy Chapter 33: Goiter Section D: Thoracic Chapter 34: Bronchopulmonary Sequestration Chapter 35: Cystic Adenomatoid Malformation Chapter 36: Other Cystic Lesions of the Chest Chapter 37: Congenital Diaphragmatic Hernia Chapter 38: Hydrothorax Chapter 39: Pulmonary Agenesis Chapter 40: Esophageal Atresia and Tracheoesophageal Fistula Section E: Cardiovascular Chapter 41: Tachyarrhythmias Chapter 42: Bradyarrhythmias Chapter 43: Atrial Septal Defects Chapter 44: Ventricular Septal Defects Chapter 45: Atrioventricular Canal Defect Chapter 46: Ebstein Anomaly Chapter 47: Hypoplastic Right Ventricle Chapter 48: Hypoplastic Left Ventricle Chapter 49: Pulmonary Stenosis and Atresia Chapter 50: Aortic Stenosis Chapter 51: Coarctation of the Aorta Chapter 52: Tetraology of Fallot Chapter 53: Double Outlet Right Ventricle Chapter 54: Truncus Arteriosus Chapter 55: Transposition of Great Arteries Chapter 56: Heterotaxy Syndrome Chapter 57: Cardiomyopathy Chapter 58: Intracardiac Tumors Section F: Abdominal-Wall Defects Chapter 59: Ectopia Cordis Chapter 60: Body-Stalk Anomaly Chapter 61: Pentalogy of Cantrell Chapter 62: Omphalocele Chapter 63: Gastroschisis Chapter 64: Cloacal Exstrophy Chapter 65: Bladder Exstrophy Section G: Gastrointestinal Tract Chapter 66: Cystic Lesions of the Abdomen Chapter 67: Choledochal Cyst Chapter 68: Ovarian Cysts Chapter 69: Intra-Abdominal Calcifications--Hepatic Chapter 70: Intra-Abdominal Calcifications Chapter 71: Pyloric Atresia and Stenosis Chapter 72: Duodenal Atresia and Senosis Chapter 73: Jejeunoileal Atresia and Stenosis Chapter 74: Colonic Atresia Chapter 75: Hirschsprung's Disease Chapter 76: Imperforate Anus Chapter 77: Echogenic Kidneys Chapter 78: Multicystic Dysplastic Kidney Chapter 79: Polycystic Kidney Disease Chapter 80: Hydronephrosis Minimal Chapter 81: Hydronephrosis: Ureteropelvic Junction Obstruction Chapter 82: Hydronephrosis--Bladder Outlet Obstruction Chapter 83: Hydronephrosis--Ectopic Ureterocele Section H: Genitourinary Tract Chapter 84: Ambiguous Genitalia Chapter 85: Persistent Cloaca Chapter 86: Renal Agenesis Chapter 87: Sirenomelia Section I: Skeletal Chapter 88: Hemivertebrae Chapter 89: Achondroplasia Chapter 90: Thanatophoric Dysplasia Chapter 91: Osteogenesis Imperfecta Chapter 92: Campomelic Dysplasia Chapter 93: Diastrophic Dysplasia Chapter 94: Ellis-van Creveld Syndrome Chapter 95: Short Rib Polydactyly Syndrome Chapter 96: Jarcho-Levin Syndrome Chapter 97: Achondrogenesis Chapter 98: Hypophosphatasia Chapter 99: Chondrodysplasia Punctata Section J: Extremities Chapter 100: Amniotic Band Syndrome Chapter 101: Arthrogryposis Chapter 102: Clinodactyly Chapter 103: Ectrodactyly Chapter 104: Polydactyly Chapter 105: Syndactyly Chapter 106: Radial Aplasia Chapter 107: Clubfoot Section K: Umbilical Cord Chapter 108: Umbilical Cord Abnormalities Chapter 109: Single Umbilical Artery Section L: Tumors Chapter 110: Cervical Teratoma Chapter 111: Liver Tumors Chapter 112: Mesoblastic Nephroma Chapter 113: Neuroblastoma Chapter 114: Retinoblastoma Chapter 115: Sacrococcygeal Teratoma Chapter 116: Wilms' Tumor Section M: Multiple Gestation Chapter 117: Malformations in Twins Chapter 118: Intrauterine Death in One Twin Chapter 119: Twin-to-Twin Transfusion Syndrome Chapter 120: Twin Reversed Arterial Perfusion Sequence Chapter 121: Conjoined Twins Chapter 122: Monoamniotic Twins Section N: Disorders of Growth Chapter 123: Intrauterine Growth Restriction Chapter 124: Overgrowth Syndromes Section O: Disorders of Amniotic Fluid Volume Chapter 125: Oligohydramnios Chapter 126: Polyhydramnios Section P: Hydrops Fetalis Chapter 127: Immune Hydrops Chapter 128: Nonimmune Hydrops Fetalis Part III: Management of Fetal Chromosome Abnormalities Chapter 129: Trisomy 13 Chapter 130: Trisomy 18 Chapter 131: Trisomy 21 Chapter 132: Triploidy Chapter 133: Other Autosomnal Aneuploidies Chapter 134: Turner Syndrome (45,X) Chapter 135: 47,XXY (Klinefelter Syndrome) Chapter 136: 47,XXX Karyotype (Triple X Syndrome, Trisomy X) Chapter 137: 47,XYY Karyotype (XYY) Chapter 138: Tetrasomy 12p (Pallister-Killian Syndrome) Chapter 139: 22q11.2 Deletion (DiGeorge Syndrome) Index
Specifications
Publisher
McGraw-Hill Education - Europe
Publication date
October 30, 2005
Pages
1004
ISBN
9780071442015
Format
Hardback

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