Embryo and Fetal Pathology: Color Atlas with Ultrasound CorrelationCambridge University Press, 2004 M05 31 - 711 pages Exhaustively illustrated in color with over 1000 photographs, figures, histopathology slides, and sonographs, this uniquely authoritative atlas provides the clinician with a visual guide to diagnosing congenital anomalies, both common and rare, in every organ system in the human fetus. It covers the full range of embryo and fetal pathology, from point of death, autopsy and ultrasound, through specific syndromes, intrauterine problems, organ and system defects to multiple births and conjoined twins. Gross pathologic findings are correlated with sonographic features in order that the reader may confirm visually the diagnosis of congenital abnormalities for all organ systems. Obstetricians, perinatologists, neonatologists, geneticists, anatomic pathologists, and all practitioners of maternal-fetal medicine will find this atlas an invaluable resource. |
Contents
Major Organ System Malformations | 102 |
Disruptions and Amnion Rupture Sequence | 275 |
Intrauterine Growth Retardation | 310 |
Fetal Hydrops and Cystic Hygroma | 321 |
Central Nervous System Defects 335 | 337 |
Craniofacial Defects | 367 |
Skeletal Abnormalities | 388 |
Cardiovascular System Defects 428 | 431 |
GenitoUrinary System | 513 |
Congenital Tumors | 546 |
Fetal and Neonatal Skin Disorders | 579 |
Intrauterine Infection | 601 |
Multiple Gestations and Conjoined Twins | 622 |
Metabolic Diseases | 635 |
Appendices | 657 |
| 679 | |
Other editions - View all
Embryo and Fetal Pathology: Color Atlas with Ultrasound Correlation Enid Gilbert-Barness No preview available - 2004 |
Common terms and phrases
abdominal absent agenesis amniotic fluid anencephaly aneuploidy anomalies aorta aortic arrow associated atresia atrial autosomal dominant autosomal recessive bilateral birth blood bone brain calcification cardiac cartilage cells chorionic chromosome cleft Clinical congenital cystic cysts deficiency developmental diagnosis diameter dilated disease disorders ducts dysplasia embryo embryopathy encephalocele evaluation facial fetus fetuses fibrosis Figure gene Genet genitalia gestational age Gilbert-Barness growth retardation heart hemorrhage holoprosencephaly hydrocephalus hydrops hypoplasia hypoplastic imaging increased infants infection intestinal intrauterine karyotype kidney lesions limb liver lung malformations maternal Meckel meconium membranes microcephaly Microscopic appearance midline multiple mutation neonatal neural tube newborn normal Obstet Gynecol occur oligohydramnios omphalocele palate Pathology Pediatr perinatal placenta polydactyly posterior pregnancy prenatal present pulmonary artery renal renal agenesis result risk septal defect skin skull sonographic stenosis syndactyly syndrome Table tissue trimester trisomy 18 trisomy 21 tumor twin Ultrasound umbilical cord usually valve vascular ventricle ventricular weeks gestation