Fetology [electronic resource] : diagnosis and management of the fetal patient / Diana W. Bianchi ... [et al.].

Contributor(s): Bianchi, Diana W | Bianchi, Diana W. Fetology | ProQuest (Firm)Material type: TextTextPublication details: New York : McGraw-Hill Medical Pub. Division, c2010. Edition: 2nd edDescription: xix, 1004 p. : ill. (some col.)Subject(s): Fetus -- Diseases | Fetus -- AbnormalitiesGenre/Form: Electronic books.DDC classification: 618.3 LOC classification: RG626 | .F465 2010Online resources: Click to View
Contents:
Prenatal imaging -- First trimester screening for aneuploidy -- Second trimester screening for aneuploidy -- Prenatal diagnostic procedures -- Fetal intervention -- Agenesis of the corpus callosum -- Anencephaly -- Arachnoid cyst -- Cerebral calcifications -- Craniosynostosis -- Dandy-walker malformation and variants -- Encephalocele -- Exencephaly/acrania -- Holoprosencephaly -- Hydranencephaly -- Hydrocephalus -- Intracranial hemorrhage -- Macrocephaly -- Myelomeningocele -- Microcephaly -- Porencephaly -- Vein of galen aneurysm -- Cleft lip and cleft palate -- Hemifacial microsomia -- Hypertelorism -- Hypotelorism -- Macroglossia -- Micrognathia and agnathia -- Microphthalmia/anophthalmia -- Congenital high airway obstruction syndrome -- Cystic hygroma in early pregnancy -- Cystic hygroma in late pregnancy -- Goiter -- Bronchopulmonary sequestration -- Cystic adenomatoid malformation -- Other cystic lesions of the chest -- Congenital diaphragmatic hernia -- Hydrothorax -- Pulmonary agenesis -- Esophageal atresia and tracheoesophageal fistula -- Tachyarrhythmias -- Bradyarrhythmias -- Atrial septal defects -- Ventricular septal defects -- Atrioventricular canal defect -- Ebstein anomaly -- Hypoplastic right ventricle -- Hypoplastic left ventricle -- Pulmonary stenosis and atresia -- Aortic stenosis -- Coarctation of the aorta -- Tetralogy of fallot -- Double outlet right ventricle -- Truncus arteriosus -- Transposition of great arteries -- Heterotaxy syndrome -- Cardiomyopathy -- Intracardiac tumors -- Ectopia cordis -- Body-stalk anomaly -- Pentalogy of cantrell -- Omphalocele -- Gastroschisis -- Cloacal exstrophy -- Bladder exstrophy -- Cystic lesions of the abdomen -- Choledochal cyst -- Ovarian cysts -- Intra-abdominal calcifications-hepatic -- Intra-abdominal calcifications -- Pyloric atresia and stenosis -- Duodenal atresia and stenosis -- Jejunoileal atresia and stenosis -- Colonic atresia -- Hirschsprung's disease -- Imperforate anus -- Echogenic kidneys -- Multicystic dysplastic kidney -- Polycystic kidney disease -- Hydronephrosis : minimal -- Hydronephrosis : ureteropelvic junction obstruction -- Hydronephrosis : bladder outlet obstruction -- Hydronephrosis : ectopic ureterocele -- Ambiguous genitalia -- Persistent cloaca -- Renal agenesis -- Sirenomelia -- Hemivertebrae -- Achondroplasia -- Thanatophoric dysplasia -- Osteogenesis imperfecta -- Camponelic dysplasia -- Diastrophic dysplasia -- Ellis-van creveld syndrome -- Short-rib polydactyly syndrome -- Jarcho-levin syndrome -- Achondrogenesis -- Hypophosphatasia -- Chondrodysplasia punctata -- Amniotic band syndrome -- Arthrogryposis -- Clinodactyly -- Ectrodactyly -- Polydactyly -- Syndactyly -- Radial aplasia -- Clubfoot -- Umbilical cord abnormalities -- Single umbilical artery -- Cervical teratoma -- Liver tumors -- Mesoblastic nephroma -- Neuroblastoma -- Retinoblastoma -- Sacrococcygeal teratoma -- Wilms' tumor -- Malformations in twins -- Intrauterine death in one twin -- Twin-to-twin transfusion syndrome -- Twin reversed arterial perfusion sequence -- Conjoined twins -- Monoamniotic twins -- Intrauterine growth restriction -- Overgrowth syndromes -- Oligohydramnios -- Polyhydramnios -- Immune hydrops -- Nonimmune hydrops fetalis -- Trisomy 13 -- Trisomy 18 -- Trisomy 21 (Down syndrome) -- Triploidy -- Other autosomal aneuploidies -- 45, X (Turner syndrome) -- 47, XXY (Klinefelter syndrome) -- 47, XXX (Triple X syndrome, Trisomy X) -- 47, XYY -- Tetrasomy 12p (Pallister-killian syndrome) -- 22q11.2 deletion (DiGeorge syndrome).
Summary: "This book was written to provide a multidisciplinary approach to the full implications of a fetal sonographic or chromosomal diagnosis--from prenatal management to long-term outcome--for an affected child. This book's intended audience consists of practioners who care for fetuses or neonates with sonographically detected anomalies, and who seek prenatal and postnatal information regarding specific conditions"--Provided by publisher.
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Holdings
Item type Current library Shelving location Call number Status Date due Barcode Item holds
Electronic books Electronic books Kuakarun Nursing Library
Processing unit Available Eb33993
Total holds: 0

Rev. ed. of: Fetology / Diana W. Bianchi, Timothy M. Crombleholme, Mary E. D'Alton. c2000.

Includes bibliographical references and index.

Prenatal imaging -- First trimester screening for aneuploidy -- Second trimester screening for aneuploidy -- Prenatal diagnostic procedures -- Fetal intervention -- Agenesis of the corpus callosum -- Anencephaly -- Arachnoid cyst -- Cerebral calcifications -- Craniosynostosis -- Dandy-walker malformation and variants -- Encephalocele -- Exencephaly/acrania -- Holoprosencephaly -- Hydranencephaly -- Hydrocephalus -- Intracranial hemorrhage -- Macrocephaly -- Myelomeningocele -- Microcephaly -- Porencephaly -- Vein of galen aneurysm -- Cleft lip and cleft palate -- Hemifacial microsomia -- Hypertelorism -- Hypotelorism -- Macroglossia -- Micrognathia and agnathia -- Microphthalmia/anophthalmia -- Congenital high airway obstruction syndrome -- Cystic hygroma in early pregnancy -- Cystic hygroma in late pregnancy -- Goiter -- Bronchopulmonary sequestration -- Cystic adenomatoid malformation -- Other cystic lesions of the chest -- Congenital diaphragmatic hernia -- Hydrothorax -- Pulmonary agenesis -- Esophageal atresia and tracheoesophageal fistula -- Tachyarrhythmias -- Bradyarrhythmias -- Atrial septal defects -- Ventricular septal defects -- Atrioventricular canal defect -- Ebstein anomaly -- Hypoplastic right ventricle -- Hypoplastic left ventricle -- Pulmonary stenosis and atresia -- Aortic stenosis -- Coarctation of the aorta -- Tetralogy of fallot -- Double outlet right ventricle -- Truncus arteriosus -- Transposition of great arteries -- Heterotaxy syndrome -- Cardiomyopathy -- Intracardiac tumors -- Ectopia cordis -- Body-stalk anomaly -- Pentalogy of cantrell -- Omphalocele -- Gastroschisis -- Cloacal exstrophy -- Bladder exstrophy -- Cystic lesions of the abdomen -- Choledochal cyst -- Ovarian cysts -- Intra-abdominal calcifications-hepatic -- Intra-abdominal calcifications -- Pyloric atresia and stenosis -- Duodenal atresia and stenosis -- Jejunoileal atresia and stenosis -- Colonic atresia -- Hirschsprung's disease -- Imperforate anus -- Echogenic kidneys -- Multicystic dysplastic kidney -- Polycystic kidney disease -- Hydronephrosis : minimal -- Hydronephrosis : ureteropelvic junction obstruction -- Hydronephrosis : bladder outlet obstruction -- Hydronephrosis : ectopic ureterocele -- Ambiguous genitalia -- Persistent cloaca -- Renal agenesis -- Sirenomelia -- Hemivertebrae -- Achondroplasia -- Thanatophoric dysplasia -- Osteogenesis imperfecta -- Camponelic dysplasia -- Diastrophic dysplasia -- Ellis-van creveld syndrome -- Short-rib polydactyly syndrome -- Jarcho-levin syndrome -- Achondrogenesis -- Hypophosphatasia -- Chondrodysplasia punctata -- Amniotic band syndrome -- Arthrogryposis -- Clinodactyly -- Ectrodactyly -- Polydactyly -- Syndactyly -- Radial aplasia -- Clubfoot -- Umbilical cord abnormalities -- Single umbilical artery -- Cervical teratoma -- Liver tumors -- Mesoblastic nephroma -- Neuroblastoma -- Retinoblastoma -- Sacrococcygeal teratoma -- Wilms' tumor -- Malformations in twins -- Intrauterine death in one twin -- Twin-to-twin transfusion syndrome -- Twin reversed arterial perfusion sequence -- Conjoined twins -- Monoamniotic twins -- Intrauterine growth restriction -- Overgrowth syndromes -- Oligohydramnios -- Polyhydramnios -- Immune hydrops -- Nonimmune hydrops fetalis -- Trisomy 13 -- Trisomy 18 -- Trisomy 21 (Down syndrome) -- Triploidy -- Other autosomal aneuploidies -- 45, X (Turner syndrome) -- 47, XXY (Klinefelter syndrome) -- 47, XXX (Triple X syndrome, Trisomy X) -- 47, XYY -- Tetrasomy 12p (Pallister-killian syndrome) -- 22q11.2 deletion (DiGeorge syndrome).

"This book was written to provide a multidisciplinary approach to the full implications of a fetal sonographic or chromosomal diagnosis--from prenatal management to long-term outcome--for an affected child. This book's intended audience consists of practioners who care for fetuses or neonates with sonographically detected anomalies, and who seek prenatal and postnatal information regarding specific conditions"--Provided by publisher.

Electronic reproduction. Ann Arbor, MI : ProQuest, 2016. Available via World Wide Web. Access may be limited to ProQuest affiliated libraries.

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