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Common malformations.
This extensively illustrated reference work is designed for health professionals who care for newborn infants including neonatologists, pediatricians, NICU nurses, pediatric neurologists, pediatric surgeons, geneticists, and genetic counselors. It describes the most common malformations and draws th...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Oxford :
Oxford University Press, USA,
2011.
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 100 | 1 | |a Holmes, Lewis B. | |
| 245 | 1 | 0 | |a Common malformations. |
| 260 | |a Oxford : |b Oxford University Press, USA, |c 2011. | ||
| 300 | |a 1 online resource (481 pages) | ||
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| 520 | |a This extensively illustrated reference work is designed for health professionals who care for newborn infants including neonatologists, pediatricians, NICU nurses, pediatric neurologists, pediatric surgeons, geneticists, and genetic counselors. It describes the most common malformations and draws the information needed for a full diagnostic evaluation and discussion of treatment options and genetic counseling from many sources. The text also covers minor anomalies, birthmarks and includes dozens of charts of anthropologic measurements, material that is needed in the initial physical examinatio. | ||
| 504 | |a Includes bibliographical references. | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a Cover; Contents; 1. The Approach to the Malformed Newborn; 2. Amniotic Bands; 3. Bowel Atresias; i. Duodenal Atresia; ii. Esophageal Atresia; iii. Imperforate Anus; iv. Jejunoileal Atresia; 4. Chromosome Abnormalities; i. Trisomy 21; ii. Trisomy 18; iii. Trisomy 13; 5. Cleft Lip and Palate; 6. Cleft Palate; 7. Club Foot; 8. Congenital Diaphragmatic Hernia; 9. Cryptorchidism; 10. Gastroschisis; 11. Heart Defects; 12. Hip Dysplasia; 13. Holoprosencephaly; 14. Hypospadias; 15. Limb Malformations; i. Polydactyly, Postaxial, Types A and B (Pedunculated Postminimus); ii. Polydactyly-Preaxial. | |
| 505 | 8 | |a Iii. Polysyndactylyiv. Longitudinal Deficiency, Preaxial: Absence/Hypoplasia of Thumb and/or Radius; v. Longitudinal Deficiency, Preaxial: Absence/Hypoplasia of Tibia and/or First Toe; vi. Longitudinal Deficiency, Postaxial: Absence/Hypoplasia of Ulna and/or Fifth Finger; vii. Longitudinal Deficiency, Postaxial: Absence/Hypoplasia of Fibula and/or Fifth Toe; viii. Split Hand/Split Foot (SHSFM); ix. Syndactyly; x. Terminal Transverse Limb Defects (TTLD) with Nubbins; xi. Central Digit Hypoplasia; 16. Microphthalmia/Anophthalmia; 17. Microtia; 18. Neural Tube Defects; i. Anencephaly. | |
| 505 | 8 | |a Ii. Cloacal Exstrophyiii. Encephalocele; iv. Iniencephaly; v. Lipomyelomeningocele; vi. Meningocele; vii. Myelomeningocele; 19. Omphalocele; 20. Renal Agenesis/Dysgenesis; 21. Skeletal Dysplasias; 22. Vertebral Anomalies: Hemivertebra; 23. Patterns of Malformations: Non-Random Clusters; i. C.H.A.R.G.E Association; ii. Hemifacial Microsomia; iii. Otocephaly; iv. Poland Anomaly; v. Urethral Obstruction: Prune Belly Syndrome; vi. VACTERL (Vater) Association; 24. Twinning; i. Acardia; ii. Conjoined Twins; iii. Sirenomelia; iv. Twin-Twin Transfusion; 25. Minor Anomalies/Normal Variations. | |
| 505 | 8 | |a 26. Birth Marks27. Anthropologic Measurements; Index; A; B; C; D; E; F; G; H; I; J; K; L; M; N; O; P; Q; R; S; T; U; V; W; X; Z. | |
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| 650 | 0 | |a Abnormalities, Human. | |
| 650 | 1 | 2 | |a Congenital Abnormalities |
| 650 | 6 | |a Malformations. | |
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| 650 | 7 | |a Abnormalities, Human |2 fast | |
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