MARC Record from harvard_bibliographic_metadata

LEADER: 08673cam a22005534a 4500
001 011385057-3
005 20131016130026.0
008 070208s2008 paua b 001 0 eng
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050 00 $aRG628.3.U58$bB46 2008
060 10 $aWQ 211$bB456u 2008
082 00 $a618.3/207543$222
100 1 $aBenacerraf, Beryl R.
245 10 $aUltrasound of fetal syndromes /$cBeryl R. Benacerraf.
250 $a2nd ed.
260 $aPhiladelphia :$bChurchill Livingstone / Elsevier,$cc2008.
300 $axvi, 650 p. :$bill. (some col.) ;$c29 cm. +$e1 DVD-ROM (4 3/4 in.)
500 $aDVD-ROM in pocket.
504 $aIncludes bibliographical references and index.
538 $aSystem requirements for Microsoft Windows: Windows 2000, XP or Vista; 800 x 600 pixels screen resolution; 16.7 million colors; 256 MB RAM; P III 500 MHz processor; DVD-ROM drive.
538 $aSystem requirements for Macintosh: OS X 10.2 or above; 800 x 600 pixels screen resolution; Millions of colors; 256 MB RAM; G3 800 MHz processor; DVD-ROM drive.
505 0 $aDifferntial dianoses. Cataract -- Microphthalmia/anophthalmia (unilateral or bilateral) -- Hypotelorism/cyclopia (extreme) -- Hypertelorism -- Choanal atresia -- Micrognathia -- Facial asymmetry -- Nasal bone hypoplasia (otherwise normal nose) -- Facial cleft -- Ear anomalies -- Abnormal head shape -- Sluid collections in the head -- Intracranial cyst -- Ventriculomegaly -- Macrocephaly -- Microcephaly -- Agenesis of the corpus callosum -- Dandy-Walker cyst or vermian hypoplasia -- Echogenic mass in the head -- Holoprosencephaly -- Neural tube defect -- Short spine -- Vertebral body segmental abnormalities (other than platyspondyly) -- Platyspondyly -- Rib abnormalities -- Mass on the surface of the fetus -- Nuchal membrane -- Nuchal thickening/cystic hygroma (first and/or second trimesters) -- Anterior abdominal wall defects -- Omphalocele -- Anterior neck mass -- Rotation of the heart -- Intrathoracic mass -- Diaphragmatic hernia -- Narrow chest -- Abdominal fluid collection or cyst -- Hyperechoic bowel -- Echogenic mass in abdomen -- Bowel obstruction -- Ascites -- Absent stomach -- Hydronephrosis -- Renal agenesis (unilateral or bilateral) -- Syndromes associated with various renal anomalies -- Absent bladder -- Distended bladder -- Suprarenal mass -- Enlarged kidneys -- GEnital anomalies -- Contractures of the extremities -- Clenched hands -- Polydactyly -- Clinodactyly -- Asymmetric lengths of extremities -- Slightly short femur -- Generalized short and bowed limbs -- Asymmetric limb reduction defects -- Short radial ray -- Club feet -- Rockerbottom feet -- Flared metaphyses or epithyses -- under-ossification of bone -- Cord cyst/mass -- Hydrops -- Decreased fetal activity -- Intrauterine growth restriction -- Enlarged placenta -- Polyhydramnios -- Oligohyframnios -- Heart defects -- Echogenic intracardiac focus -- Abnormal heart appearance.
505 0 $aEnlarged right side of hte heart (compared with the left) -- Smaller right side of the heart (compared with the left) -- Enlarged left side of the heart (compared with the right) -- Smaller left side of the heart (compared with the right) -- Single great vessel -- Single ventricle -- Syndromes. Syndromes featuring growth restriction. Cornelia de Lange syndrome -- Noonan syndrome -- Russell-Silver syndrome -- Seckel syndrome -- Smith-Lemli-Opitz sydrome -- Syndromes featuring fetal overgrowth. Beckwith-Wiedermann syndrome -- Maternal diabetes -- Perlman syndrome -- Syndromes featuring primarily facial anomalies. Branchio-ocular-facial syndrome -- Cataracts -- Cerebrocostomandibular syndrome -- Cleft lip and palate -- Fraser syndrome -- Goldenhar syndrome -- Medial cleft face syndrome -- Microphthalmia/anophthalmia -- Nager syndrome -- Oral-facial-digital syndrome, type I (OFD1) -- Oral-facial-digital syndrome, type II (Mohr syndrome) -- Pierre Robin syndrome -- Shprintzen syndrome -- Strickler syndrome -- Treacher Collins syndrome -- Van der Woude syndrome -- Syndromes featuring primarily brain anomalies. Aicardia syndrome -- Gorlin syndrome -- Hydrolethalis -- Joubert syndrome -- Meckel-Gruber syndrome -- Microcephaly -- Miller-Dieker syndrome (lissencephaly, type I) -- Neu-Laxova syndrome -- Septo-optic syndrome -- Walker-Warburg syndrome -- X-linked hydrocephalus syndrome -- Limb abnormalities. Adams-Oliver syndrome -- Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome -- Fanconi anemia -- Femoral hyopplasi-unusual facies syndrome -- Femur-fibula-ulna (FFU) syndrome -- Freeman-Sheldon (whistling face) syndrome -- Holt-oram syndrome.
505 0 $aLarsen syndrome -- Multiple pterygium syndrome (lethal type) -- Roberts' syndrome -- Thrombocytopenia-absent radius (TAR) syndrome -- Skeletal dysplasias. Achondrogenesis -- Achodroplasia -- Atelosteogenesis, type I -- Camptomelic dysplasia -- Chondrodysplasia punctata -- Cleidocranial dysostosis -- Diastrophic dysplasia -- Ellis-van Creveld syndrome -- Hypochondroplasia -- Hypophosphatasia of the lethal type -- Jeune thoracic dystrophy -- Kniest syndrome -- Majewski syndrome -- Metatrophic dysplasia -- Osteopetrosis (lethal type) -- Short rib-polydactyly syndromes (SRPS) types I (Saldino-Noonan) and III (Naumoff) -- Spondyloepiphyseal dysplasia congenita -- Thanatophoric dysplasia -- Syndromes featuring primarily craniosynostosis. Antley-bixter syndrome -- Apert syndrome -- Carpenter syndrome -- Couzon syndrome -- Pfeiffer syndrome -- Saethre-Chotzen syndrome -- Miscellaneous syndromes. Cystic fibrosis -- Fryns syndrome -- Infantile polycystic kidney disease -- Jarcho-Levin syndrome -- Syndromes featuring primarily soft-tissue anomalies. Alpha-thalassernia -- Aplasia cutis congenita (ACC) -- Harlequin syndrome -- Klippel-Trenaunay-Weber syndrome -- Marfan syndrome -- Osteogenesis imperfecta -- Proteus syndrome -- Tuberous syndrome -- Sequence and associations. Amniotic band sequence -- Arthrogryposis -- Cardiosplenic syndromes (asplenia/polyspenia; heterotaxy) -- Caudal regression syndrome and sirenomelia -- Cerebro-occulo-facio-skeletal (CODS) syndrome -- CHARGE association -- Congenital adrenal hyperplasia -- Congenital high airway obstruction syndrome (CHAOS) -- Cloacal extrophy sequence -- Holoprosencephaly sequence -- Idiopathic arterial calcification of infancy.
505 0 $aKlippel-Feil syndrome -- MURCS association -- Opitz syndrome -- Pena Shokeir syndrome -- Pentalogy of cantrell -- Prune-belly syndrome -- Renal agenesis (Potter syndrome) -- Scimitar syndrome -- Spinal dysraphism -- VATER association -- Teratogens. Antibiotics -- Anticancer agents -- Anticoagulants -- Anticonvulsant drugs -- Anithyroid agents -- Hormones -- Tranquilizers and antidepressants -- Miscellaneous -- Maternal infections -- Syndromes featuring chromosomal anomalies. Cri-du-chat (distal 5p deletion syndrome) -- Deletion 4p (Wolf-Hirschhorn syndrome) -- Deletion 11q (Jacobsen syndrome) -- DiGeorge syndrome -- Tetrasomy (Pallister-Killiam syndrome) -- Triploidy -- Trisomy 9 -- Trisomy 10 -- Trisomy 13 (Patau syndrome) -- Trisomy 18 (Edwards syndrome) -- Trisomy 21 (downs syndrome) -- Trisomy 22 -- XO syndrome (Turner syndrome) -- Tumors. Cystic hygroma/lymphangioma -- Hemangioma -- Neuroblastoma -- Teratoma.
520 $aThis book on prenatal diagnosis details the most common sonographically detectable fetal syndromes. It has an easy-to-follow approach of using lists and patterns of malformations to generate a differential diagnosis of the possible syndrome involved. The reader is then led to the more detailed description of each syndrome to determine the exact final diagnosis. The new edition incorporates 3D ultrasound throughout the book, as well as 20 syndromes not previously covered.
650 0 $aFetus$xUltrasonic imaging.
650 0 $aFetus$xAbnormalities$xDiagnosis.
650 0 $aFetus$xDiseases$xDiagnosis.
650 0 $aPrenatal diagnosis.
650 12 $aFetal Diseases$xultrasonography.
650 22 $aCongenital Abnormalities$xultrasonography.
650 22 $aDiagnosis, Differential.
650 22 $aFetus$xabnormalities.
650 22 $aUltrasonography, Prenatal.
655 7 $aDVD-ROMs.$2local
650 22 $aCongenital Abnormalites$xultrasonography.
650 6 $aFœtus$xÉchographie.
650 6 $aFœtus$xMalformations$xDiagnostic.
650 6 $aFœtus$xMaladies$xDiagnostic.
650 6 $aDiagnostics prénatals.
988 $a20080213
906 $0OCLC