Congenital Malformations: Evidence-Based Evaluation and ManagementMcGraw Hill Professional, 6 nov 2007 - 364 páginas A concise, clinically-focused guide to the evaluation and management of infants with congenital malformations Congenital Malformations is a comprehensive, practical text that highlights key perspectives on the medical management of infants with malformations. With its convenient system-based organization and evidence-based approach, this clinically-focused guide is designed to optimize the utilization of limited diagnostic resources. Easy-to-follow algorithms and tables enable you to rapidly identify and manage the many different malformations that commonly present in clinical practice, such as cleft lip, cardiac septal defects, and skeletal dysplasias. Features:
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Índice
Central Nervous System Malformations | 39 |
Craniofacial Malformations | 91 |
Respiratory Malformations | 133 |
Cardiac Malformations | 171 |
Gastrointestinal Malformations | 215 |
Renal Malformations | 251 |
Skeletal Malformations | 283 |
Miscellaneous Malformations | 331 |
Glossary of Genetic Terms | 363 |
Web Resources | 375 |
Index | 379 |
Otras ediciones - Ver todo
Congenital Malformations: Evidence-Based Evaluation and Management Praveen Kumar,Barbara Burton Vista previa restringida - 2007 |
Congenital Malformations: Evidence-Based Evaluation and Management Praveen Kumar,Barbara Burton Vista de fragmentos - 2007 |
Términos y frases comunes
abdominal aortic arthrogryposis associated anomalies ASSOCIATED MALFORMATIONS Autosomal dominant Autosomal recessive bilateral birth defects cardiac defects cataracts cells chromosomal abnormality cleft lip cleft palate CLINICAL PRESENTATION coloboma common congenital anomalies congenital heart congenital malformations contractures corpus callosum craniofacial craniosynostosis cryptorchidism cystic hygroma deletion disorder drome dysmorphic ear anomalies etiology evaluation facial family history fetal fetus fistula gene GENETIC COUNSELING genital gestation heart defects Hirschsprung disease holoprosencephaly horseshoe kidney hydrocephalus hypertelorism hypoplasia incidence infants inheritance intrauterine isolated IUGR karyotype lesions limb reduction defects lung maternal microcephaly multiple mutation neonatal neural tube defects newborn normal occult spinal dysraphism omphalocele patients Pediatr polydactyly posterior pregnancy prenatal diagnosis pulmonary agenesis pulmonary hypoplasia recurrence risk renal agenesis renal ultrasound reported respiratory retardation septal defect single umbilical artery skeletal dysplasias spina bifida stenosis studies Surg syndactyly Syndromes Associated Table tion Trisomy ultrasound umbilical artery unilateral valve ventricular X-linked