Rosenstein, B: STRUCTURAL FETAL ABNORMALITIES

Rosenstein, B: STRUCTURAL FETAL ABNORMALITIES
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9780323014762
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This 2nd Edition presents a comprehensive, integrated approach to the detection and treatment of 100 of the most common fetal anomalies, including anomalies of the limbs, heart, central nervous, genitourinary, and gastrointestinal systems, as well as alphafeta-protein, multisystem, and chromosomal abnormalities. The cardiac section has been completely revised, with discussions of 10 new entities and useful, well-illustrated tips on performing fetal echocardiography. Sixteen new entities associated with other parts of the body have also been added. All chapters in this edition are extensively revised to present the latest information.
Chromosomes 1. Triploidy 2. Trisomy 13 3. Trisomy 18 4. Trisomy 21 5. Turner Syndrome Central Nervous System 6. Agenesis of the Corpus Callosum (ACC) 7. Acencephaly 8. Aqueductal Stenosis 9. Arachnoid Cyst 10. Cauda A/Dysplasia (Regression) Sequence 11. Cranial Tumors other than Intracranial Teratoma 12. Craniosynostosis 13. Dandy Walker Malformation 14. Diastematomyelia 15. Encephalocele 16. Holoprosencephaly 17. Hydranencephaly 18. Iniencephaly 19. Intracranial Hemorrhage 20. Intracranial Teratoma 21. Microcephaly 22. Porencephaly, and Schizencephaly 23. Spinal Dysraphism 24. Vein of Galen Malformation Cardiac Entities 25. Transposition of the Great Arteries 26. Tetraology of Falott 27. Ebstein's Anomaly 28. Tricuspid Valve Atresia 29. Critical Valvar Pulmonary Stenosis and Pulmonary Atresia 30. Critical Valvar Aortic Stenosis 31. Hypoplastic Left Heart Syndrome 32. Aortic Coarctation 33. Ventricle Septal Defect 34. Atrioventricular Canal Defects 35. Truncus Arteriosus 36. Double Inlet Ventricle 37. Double Outlet Right Ventricle 38. Cardia Arrhythmias (tachycardia and extrasystoles) 39. Hypertrophic Cardiomyopathy 40. Heterotaxy Syndrome 41. Ectopia Cordis, Pentalogy of Cantrell The Genitourinary Tract 42. Adrenal Hemorrage 43. Exstrophy of the Bladder 44. Cloacal Abnormalities 45. Hydronephrosis (Ureteropelvic Junction Obstruction (UPJ and Reflux) 46. Hydrocolpus, Hydrometrocolpus 47. Autosomal Recessive Polycystic Kidney Disease (Infantile Polycystic Kidney Disease) 48. Mesoblastic Nephroma 49. Multicystic (Dysplastic) Kidney 50. Neuroblastoma 51. Ovarian Cysts 52. Posterior Urethral Valves (PUV) 53. Renal Agenesis 54. Sacrococcygeal Teratoma (SCT) 55. Sirenomelia 56. Ureterocele Chest 57. Cystic Adenomatoid Malformation of the Lung 58. Diaphragmatic Hernia 59. Esophageal Atresia 60. Pleural Effusion (Fetal Hydrothorax) 61. Pulmonary Sequestration 62. Tracheal/Laryngeal Atresia or Chaos (Congenital High Airway Obstruction Syndrome) Gastrointestinal System 63. Anal Atresia (Imperforate Anus) 64. Duodenal Atresia 65. Gastrointestinal Atresia 66. Gastroschesis 67. Hepatic Tumors 68. Meconium Cyst (Peritonitis) 69. Meconium Ileus 70. Omphalocele Neck and Face 71. Cleft Lip and Palate 72. Cystic Hygroma 73. Facial Asymmetry 74. Pierre Robin Syndrome 75. Thyroid Enlargement/Goiter 76. Treacher Collins Syndrome (Mandibulofacial Dysostosis (MFD)) Skeletal Abnormalities 77. Achondrogenesis 78. Achondroplasia 79. Amniotic Band Syndrom 80. Arthrogryposis 81. Campomelic Dysplasia 82. Club and Rocker-Bottom Feet (Vertical Talus) 83. Diastrophic Dysplasia 84. Focal Femoral Hypoplasia 85. Jeune Thoracic Dystrophy (Asphyxiating Thoracic Dystrophy) 86. Klippel Trenaunay Weber Syndrome (KTWS) 87. Limb Body Wall Complex (LBWC) (Body Stalk Complex, Cyllosomas) 88. Multiple Pteryguim Syndrome 89. Osteogenesis Imperfecta (OI) 90. Polydactyly 91. Radial Ray Problems (Radial Ray A/Hypoplasia) 92. Thanatophoric Dwarfism (Dysplasia) Infections 93. Cytomegalic Inclusion Disease (CMV) 94. Parvovirus (Firth Disease) 95. Congenital Syphilis 96. Toxoplasmosis 97. Varicella Infection (Varicella-Zoster Virus) Drugs 98. Fetal Alcohol Syndrome (FAS) 99. Anti-Seizure Drugs (Phenytoin, Carbamazephine, Valporic Acid and Phenobarbital) 100. Illegal Drugs (Cocaine, Heroine) Syndromes 101. Beckwith Wiedermann Syndrome 102. Deletion 22Q11.2 Syndrome (DiGeorge Syndrome, Velocardiofacial Syndrome, Shprintzen Syndrome) 103. Fryns Syndrome 104. Meckel Gruber (Dysencephalia Splanchocystica) 105. Pena-Shoker Phenotype (Fetal Akinesia/Hypokinesia Sequence) 106. Smith-Lemli-Opitz Syndrome 107. Tuberous Sclerosis 108. Vacterl Association Twins 109. Acardiac Twin (Acardiac Monster) Holoacardius Twin Reversed Arterial Perfusion Sequence (TRAP) 110. Conjoined Twins 111. Intrauterine Growth Restriction or Retardation (UIGR) 112. Monoamniotic Twins 113. Stuck Twin 114. Twin-Twin Transfusion Miscellaneous Abnormalities 115. Chorioangioma 116. Non-Immune Hydrops Fetalis 117. Rhesus Imcompatibility Abnormal Sonographic Findings 118. Amniotic Membranes 119. Cord Cyst 120. IUGR 121. Macrosomia 122. Oligohydramios 123. Polyhydramnios

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