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Birth defects [[electronic resource] ] : issues on prevention and promotion / / Nevin Hotun Sahin and Ilkay Gungor
Birth defects [[electronic resource] ] : issues on prevention and promotion / / Nevin Hotun Sahin and Ilkay Gungor
Autore Sahin Nevin Hotun
Pubbl/distr/stampa New York, : Nova Science Publishers, c2010
Descrizione fisica 1 online resource (141 p.)
Disciplina 616/.043
Altri autori (Persone) GungorIlkay
Collana Health care issues, costs and access
Soggetto topico Abnormalities, Human - Prevention
Soggetto genere / forma Electronic books.
ISBN 1-61728-803-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Demographical and social factors -- Genetic history and obstetric factors -- Maternal health conditions -- Nutrition -- Teratogens -- Fertility regulation and preconceptional care -- Prevention strategies and the roles of healthcare professionals.
Record Nr. UNINA-9910461721703321
Sahin Nevin Hotun  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Birth defects [[electronic resource] ] : issues on prevention and promotion / / Nevin Hotun Sahin and Ilkay Gungor
Birth defects [[electronic resource] ] : issues on prevention and promotion / / Nevin Hotun Sahin and Ilkay Gungor
Autore Sahin Nevin Hotun
Pubbl/distr/stampa New York, : Nova Science Publishers, c2010
Descrizione fisica 1 online resource (141 p.)
Disciplina 616/.043
Altri autori (Persone) GungorIlkay
Collana Health care issues, costs and access
Soggetto topico Abnormalities, Human - Prevention
ISBN 1-61728-803-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Demographical and social factors -- Genetic history and obstetric factors -- Maternal health conditions -- Nutrition -- Teratogens -- Fertility regulation and preconceptional care -- Prevention strategies and the roles of healthcare professionals.
Record Nr. UNINA-9910790127503321
Sahin Nevin Hotun  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Birth defects [[electronic resource] ] : issues on prevention and promotion / / Nevin Hotun Sahin and Ilkay Gungor
Birth defects [[electronic resource] ] : issues on prevention and promotion / / Nevin Hotun Sahin and Ilkay Gungor
Autore Sahin Nevin Hotun
Pubbl/distr/stampa New York, : Nova Science Publishers, c2010
Descrizione fisica 1 online resource (141 p.)
Disciplina 616/.043
Altri autori (Persone) GungorIlkay
Collana Health care issues, costs and access
Soggetto topico Abnormalities, Human - Prevention
ISBN 1-61728-803-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Demographical and social factors -- Genetic history and obstetric factors -- Maternal health conditions -- Nutrition -- Teratogens -- Fertility regulation and preconceptional care -- Prevention strategies and the roles of healthcare professionals.
Record Nr. UNINA-9910811925903321
Sahin Nevin Hotun  
New York, : Nova Science Publishers, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Human malformations and related anomalies / / edited by Roger E. Stevenson [and five others]
Human malformations and related anomalies / / edited by Roger E. Stevenson [and five others]
Edizione [Third edition.]
Pubbl/distr/stampa New York, New York : , : Oxford University Press, , 2016
Descrizione fisica 1 online resource (1001 p.)
Disciplina 616.042
Collana Oxford Monographs on Medical Genetics
Soggetto topico Abnormalities, Human - Prevention
Abnormalities, Human - Research
Soggetto genere / forma Electronic books.
ISBN 0-19-938605-6
0-19-938604-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; OXFORD MONOGRAPHS ON MEDICAL GENETICS; HUMAN MALFORMATIONS AND RELATED ANOMALIE; CONTENTS; PREFACE; ACKNOWLEDGMENTS; CONTRIBUTORS; INTRODUCTION; I.1. Nomenclature; I.2. Etiology and Pathogenesis; I.3. Classification and Coding; I.4. Genetic Causes of Congenital Anomalies; I.5. Environmental Causes of Congenital Anomalies; I.6. Human Anomalies with Unknown Causes; I.7. Detection, Diagnosis, Evaluation, Management; 1 | LIMBS; Introduction; 1.1. Limb Deficiency; 1.1a. Absence of Limb; 1.1b. Absent Radius; 1.1c. Absent Ulna; 1.1d. Absence and Hypoplasia of the Humerus
1.1e. Absence and Hypoplasia of the Tibia1.1f. Absence and Hypoplasia of the Fibula ; 1.1g. Absence and Hypoplasia of the Femur; 1.1h. Terminal Transverse Limb Deficiency; 1.2. Synostosis; 1.2a. Carpal Coalition and Tarsal Coalition; 1.2b. Metacarpophalangeal and Metatarsophalangeal Synostosis; 1.2c. Proximal Symphalangism; 1.2d. Distal Symphalangism; 1.2e. Humeroradial Synostosis; 1.2f. Radioulnar Synostosis; 1.2g. Tibiofibular Synostosis; 1.2h. Sirenomelia; 1.3. Constriction Rings; 1.4. Excessive Partitions, Duplications, and Accessory Bones; 1.5. Bowing of Long Bones; 1.6. Short Stature
1.7. Tall Stature1.8. Limb Overgrowth; 1.9. Increased Bone Density; 1.10. Decreased Bone Density; 1.11. Osteolysis; 1.12. Anomalies of the Patella; 1.13. Arthrogryposis; 1.13a. Amyoplasia; 1.13b. Distal Arthrogryposis; 1.13c. Fetal Akinesia Phenotype; 1.13d. Pterygium; 2 | HANDS AND FEET; Introduction; 2.1. Polydactyly; 2.1a. Preaxial Polydactyly; 2.1b. Postaxial Polydactyly; 2.1c. Mesoaxial Polydactyly; 2.2. Syndactyly; 2.2a. Syndactyly Type I; 2.2b. Syndactyly Type II; 2.2c. Syndactyly Type III; 2.2d. Syndactyly Type IV; 2.2e. Syndactyly Type V; 2.2f. Complete Syndactyly
2.2g. Cenani-Lenz Syndactyly2.2h. Symbrachydactyly; 2.3. Brachydactyly; 2.3a. Brachydactyly Type A1; 2.3b. Brachydactyly Type A2; 2.3c. Brachydactyly Type A3; 2.3d. Brachydactyly Type B; 2.3e. Brachydactyly Type C; 2.3f. Brachydactyly Type D; 2.3g. Brachydactyly Type E; 2.4. Osseous Deficiencies of the Hands and Feet; 2.4a. Preaxial Deficiency; 2.4b. Postaxial Deficiency; 2.5. Terminal Transverse Deficiency; 2.6. Split-Hand/Foot Malformation; 2.7. Macrodactyly; 2.8. Camptodactyly; 2.9. Clubfoot; 3 | PECTORAL AND PELVIC GIRDLES; Introduction; 3.1. Clavicular Hypoplasia or Aplasia
3.2. Clavicular Pseudoarthrosis3.3. Altered Shape and Other Abnormalities of the Clavicle; 3.4. Sprengel Anomaly; 3.5. Glenoid Hypoplasia; 3.6. Anomalies of the Pelvic Bones; 3.7. Developmental Dysplasia of the Hip; 3.8. Coxa Vara; 3.9. Coxa Valga; 4 | SPINE AND THORACIC CAGE; Introduction; 4.1. Occipitalization of the Atlas; 4.2. Aplasia/Hypoplasia of the Odontoid Process of the Axis; 4.3. Klippel-Feil Anomaly; 4.4. Segmentation Defects of the Vertebrae; 4.5. Altered Vertebral Body Contour; 4.6. Sagittal Clefts of the Vertebrae; 4.7. Coronal Clefts of the Vertebrae
4.8. Spondylolysis and Spondylolisthesis
Record Nr. UNINA-9910461056003321
New York, New York : , : Oxford University Press, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Human malformations and related anomalies / / edited by Roger E. Stevenson [and five others]
Human malformations and related anomalies / / edited by Roger E. Stevenson [and five others]
Edizione [Third edition.]
Pubbl/distr/stampa New York, New York : , : Oxford University Press, , 2016
Descrizione fisica 1 online resource (1001 p.)
Disciplina 616.042
Collana Oxford Monographs on Medical Genetics
Soggetto topico Abnormalities, Human - Prevention
Abnormalities, Human - Research
ISBN 0-19-938605-6
0-19-938604-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; OXFORD MONOGRAPHS ON MEDICAL GENETICS; HUMAN MALFORMATIONS AND RELATED ANOMALIE; CONTENTS; PREFACE; ACKNOWLEDGMENTS; CONTRIBUTORS; INTRODUCTION; I.1. Nomenclature; I.2. Etiology and Pathogenesis; I.3. Classification and Coding; I.4. Genetic Causes of Congenital Anomalies; I.5. Environmental Causes of Congenital Anomalies; I.6. Human Anomalies with Unknown Causes; I.7. Detection, Diagnosis, Evaluation, Management; 1 | LIMBS; Introduction; 1.1. Limb Deficiency; 1.1a. Absence of Limb; 1.1b. Absent Radius; 1.1c. Absent Ulna; 1.1d. Absence and Hypoplasia of the Humerus
1.1e. Absence and Hypoplasia of the Tibia1.1f. Absence and Hypoplasia of the Fibula ; 1.1g. Absence and Hypoplasia of the Femur; 1.1h. Terminal Transverse Limb Deficiency; 1.2. Synostosis; 1.2a. Carpal Coalition and Tarsal Coalition; 1.2b. Metacarpophalangeal and Metatarsophalangeal Synostosis; 1.2c. Proximal Symphalangism; 1.2d. Distal Symphalangism; 1.2e. Humeroradial Synostosis; 1.2f. Radioulnar Synostosis; 1.2g. Tibiofibular Synostosis; 1.2h. Sirenomelia; 1.3. Constriction Rings; 1.4. Excessive Partitions, Duplications, and Accessory Bones; 1.5. Bowing of Long Bones; 1.6. Short Stature
1.7. Tall Stature1.8. Limb Overgrowth; 1.9. Increased Bone Density; 1.10. Decreased Bone Density; 1.11. Osteolysis; 1.12. Anomalies of the Patella; 1.13. Arthrogryposis; 1.13a. Amyoplasia; 1.13b. Distal Arthrogryposis; 1.13c. Fetal Akinesia Phenotype; 1.13d. Pterygium; 2 | HANDS AND FEET; Introduction; 2.1. Polydactyly; 2.1a. Preaxial Polydactyly; 2.1b. Postaxial Polydactyly; 2.1c. Mesoaxial Polydactyly; 2.2. Syndactyly; 2.2a. Syndactyly Type I; 2.2b. Syndactyly Type II; 2.2c. Syndactyly Type III; 2.2d. Syndactyly Type IV; 2.2e. Syndactyly Type V; 2.2f. Complete Syndactyly
2.2g. Cenani-Lenz Syndactyly2.2h. Symbrachydactyly; 2.3. Brachydactyly; 2.3a. Brachydactyly Type A1; 2.3b. Brachydactyly Type A2; 2.3c. Brachydactyly Type A3; 2.3d. Brachydactyly Type B; 2.3e. Brachydactyly Type C; 2.3f. Brachydactyly Type D; 2.3g. Brachydactyly Type E; 2.4. Osseous Deficiencies of the Hands and Feet; 2.4a. Preaxial Deficiency; 2.4b. Postaxial Deficiency; 2.5. Terminal Transverse Deficiency; 2.6. Split-Hand/Foot Malformation; 2.7. Macrodactyly; 2.8. Camptodactyly; 2.9. Clubfoot; 3 | PECTORAL AND PELVIC GIRDLES; Introduction; 3.1. Clavicular Hypoplasia or Aplasia
3.2. Clavicular Pseudoarthrosis3.3. Altered Shape and Other Abnormalities of the Clavicle; 3.4. Sprengel Anomaly; 3.5. Glenoid Hypoplasia; 3.6. Anomalies of the Pelvic Bones; 3.7. Developmental Dysplasia of the Hip; 3.8. Coxa Vara; 3.9. Coxa Valga; 4 | SPINE AND THORACIC CAGE; Introduction; 4.1. Occipitalization of the Atlas; 4.2. Aplasia/Hypoplasia of the Odontoid Process of the Axis; 4.3. Klippel-Feil Anomaly; 4.4. Segmentation Defects of the Vertebrae; 4.5. Altered Vertebral Body Contour; 4.6. Sagittal Clefts of the Vertebrae; 4.7. Coronal Clefts of the Vertebrae
4.8. Spondylolysis and Spondylolisthesis
Record Nr. UNINA-9910797775003321
New York, New York : , : Oxford University Press, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Human malformations and related anomalies / / edited by Roger E. Stevenson [and five others]
Human malformations and related anomalies / / edited by Roger E. Stevenson [and five others]
Edizione [Third edition.]
Pubbl/distr/stampa New York, New York : , : Oxford University Press, , 2016
Descrizione fisica 1 online resource (1001 p.)
Disciplina 616.042
Collana Oxford Monographs on Medical Genetics
Soggetto topico Abnormalities, Human - Prevention
Abnormalities, Human - Research
ISBN 0-19-938605-6
0-19-938604-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover; OXFORD MONOGRAPHS ON MEDICAL GENETICS; HUMAN MALFORMATIONS AND RELATED ANOMALIE; CONTENTS; PREFACE; ACKNOWLEDGMENTS; CONTRIBUTORS; INTRODUCTION; I.1. Nomenclature; I.2. Etiology and Pathogenesis; I.3. Classification and Coding; I.4. Genetic Causes of Congenital Anomalies; I.5. Environmental Causes of Congenital Anomalies; I.6. Human Anomalies with Unknown Causes; I.7. Detection, Diagnosis, Evaluation, Management; 1 | LIMBS; Introduction; 1.1. Limb Deficiency; 1.1a. Absence of Limb; 1.1b. Absent Radius; 1.1c. Absent Ulna; 1.1d. Absence and Hypoplasia of the Humerus
1.1e. Absence and Hypoplasia of the Tibia1.1f. Absence and Hypoplasia of the Fibula ; 1.1g. Absence and Hypoplasia of the Femur; 1.1h. Terminal Transverse Limb Deficiency; 1.2. Synostosis; 1.2a. Carpal Coalition and Tarsal Coalition; 1.2b. Metacarpophalangeal and Metatarsophalangeal Synostosis; 1.2c. Proximal Symphalangism; 1.2d. Distal Symphalangism; 1.2e. Humeroradial Synostosis; 1.2f. Radioulnar Synostosis; 1.2g. Tibiofibular Synostosis; 1.2h. Sirenomelia; 1.3. Constriction Rings; 1.4. Excessive Partitions, Duplications, and Accessory Bones; 1.5. Bowing of Long Bones; 1.6. Short Stature
1.7. Tall Stature1.8. Limb Overgrowth; 1.9. Increased Bone Density; 1.10. Decreased Bone Density; 1.11. Osteolysis; 1.12. Anomalies of the Patella; 1.13. Arthrogryposis; 1.13a. Amyoplasia; 1.13b. Distal Arthrogryposis; 1.13c. Fetal Akinesia Phenotype; 1.13d. Pterygium; 2 | HANDS AND FEET; Introduction; 2.1. Polydactyly; 2.1a. Preaxial Polydactyly; 2.1b. Postaxial Polydactyly; 2.1c. Mesoaxial Polydactyly; 2.2. Syndactyly; 2.2a. Syndactyly Type I; 2.2b. Syndactyly Type II; 2.2c. Syndactyly Type III; 2.2d. Syndactyly Type IV; 2.2e. Syndactyly Type V; 2.2f. Complete Syndactyly
2.2g. Cenani-Lenz Syndactyly2.2h. Symbrachydactyly; 2.3. Brachydactyly; 2.3a. Brachydactyly Type A1; 2.3b. Brachydactyly Type A2; 2.3c. Brachydactyly Type A3; 2.3d. Brachydactyly Type B; 2.3e. Brachydactyly Type C; 2.3f. Brachydactyly Type D; 2.3g. Brachydactyly Type E; 2.4. Osseous Deficiencies of the Hands and Feet; 2.4a. Preaxial Deficiency; 2.4b. Postaxial Deficiency; 2.5. Terminal Transverse Deficiency; 2.6. Split-Hand/Foot Malformation; 2.7. Macrodactyly; 2.8. Camptodactyly; 2.9. Clubfoot; 3 | PECTORAL AND PELVIC GIRDLES; Introduction; 3.1. Clavicular Hypoplasia or Aplasia
3.2. Clavicular Pseudoarthrosis3.3. Altered Shape and Other Abnormalities of the Clavicle; 3.4. Sprengel Anomaly; 3.5. Glenoid Hypoplasia; 3.6. Anomalies of the Pelvic Bones; 3.7. Developmental Dysplasia of the Hip; 3.8. Coxa Vara; 3.9. Coxa Valga; 4 | SPINE AND THORACIC CAGE; Introduction; 4.1. Occipitalization of the Atlas; 4.2. Aplasia/Hypoplasia of the Odontoid Process of the Axis; 4.3. Klippel-Feil Anomaly; 4.4. Segmentation Defects of the Vertebrae; 4.5. Altered Vertebral Body Contour; 4.6. Sagittal Clefts of the Vertebrae; 4.7. Coronal Clefts of the Vertebrae
4.8. Spondylolysis and Spondylolisthesis
Record Nr. UNINA-9910809212603321
New York, New York : , : Oxford University Press, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui