Common malformations.

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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...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Holmes, Lewis B.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Oxford : Oxford University Press, USA, 2011.
Temas:
Abnormalities, Human.
Congenital Abnormalities
Malformations.
MEDICAL > Nursing > Pediatric & Neonatal.
MEDICAL > Perinatology & Neonatology.
Abnormalities, Human
Acceso en línea:Texto completo
Tabla de Contenidos:
  • 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.
  • 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.
  • 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.
  • 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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