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Congenital malformations : evidence-based evaluation and management / editors, Praveen Kumard and Barbara K. Burton.

Contributor(s): Publication details: New York : McGraw-Hill Medical, c2008.Description: xv, 390 p. : ill. ; 25 cmISBN:
  • 9780071471893 (pbk. : alk. paper)
  • 0071471898 (pbk. : alk. paper)
Subject(s): DDC classification:
  • QS 675 22 C7
LOC classification:
  • RG626 .C62 2008
Online resources:
Contents:
Dysmorphology -- Assessment of an infant with a congenital malformation -- Genetic counseling: principles and practices -- Spina bifida -- Anencephaly -- Encephalocele -- Holoprosencephaly -- Hydrocephalus -- Dandy-Walker malformation -- Chiari malformations -- Agenesis of the corpus callosum -- Craniosynostosis -- Cleft lip and palate -- Micrognathia -- Congenital anomalies associated with facial asymmetry -- Ear anomalies -- Choanal atresia -- Coloboma -- Cataract -- Congenital high airway obstruction syndrome -- Pulmonary agenesis -- Pulmonary hypoplasia -- Congenital cystic adenomatoid malformations -- Congenital diaphragmatic hernia -- Congenital hydrothorax -- Congenital pulmonary lymphangiectasia -- Septal defects -- Conotruncal heart defects -- Right ventricular outflow tract obstructive defects -- Left ventricular outflow tract obstructive defects -- Dextrocardia -- Cardiomyopathy -- Esophageal atresia and tracheoesophageal fistula -- Duodenal atresia -- Anorectal malformations -- Hirschsprung disease -- Omphalocele -- Gastroschisis -- Renal agenesis -- Horseshoe kidney -- Renal cystic diseases -- Posterior urethral valves -- Polydactyly -- Syndactyly -- Limb reduction defects -- Skeletal dysplasias -- Arthrogryposis -- Single umbilical artery -- Sacral dimple and other cutaneous markers of occult spinal dysraphism -- Hemihyperplasia and overgrowth disorders -- Cystic hygroma.
Item type: كتاب
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كتاب كتاب الطب QS 675 C7 (Browse shelf(Opens below)) Available مكتبة كلية طب الموصل

Includes bibliographical references and index.

Dysmorphology -- Assessment of an infant with a congenital malformation -- Genetic counseling: principles and practices -- Spina bifida -- Anencephaly -- Encephalocele -- Holoprosencephaly -- Hydrocephalus -- Dandy-Walker malformation -- Chiari malformations -- Agenesis of the corpus callosum -- Craniosynostosis -- Cleft lip and palate -- Micrognathia -- Congenital anomalies associated with facial asymmetry -- Ear anomalies -- Choanal atresia -- Coloboma -- Cataract -- Congenital high airway obstruction syndrome -- Pulmonary agenesis -- Pulmonary hypoplasia -- Congenital cystic adenomatoid malformations -- Congenital diaphragmatic hernia -- Congenital hydrothorax -- Congenital pulmonary lymphangiectasia -- Septal defects -- Conotruncal heart defects -- Right ventricular outflow tract obstructive defects -- Left ventricular outflow tract obstructive defects -- Dextrocardia -- Cardiomyopathy -- Esophageal atresia and tracheoesophageal fistula -- Duodenal atresia -- Anorectal malformations -- Hirschsprung disease -- Omphalocele -- Gastroschisis -- Renal agenesis -- Horseshoe kidney -- Renal cystic diseases -- Posterior urethral valves -- Polydactyly -- Syndactyly -- Limb reduction defects -- Skeletal dysplasias -- Arthrogryposis -- Single umbilical artery -- Sacral dimple and other cutaneous markers of occult spinal dysraphism -- Hemihyperplasia and overgrowth disorders -- Cystic hygroma.