Common malformations.
Holmes, Lewis B,
Common malformations. - 1 online resource (481 pages)
Includes bibliographical references.
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; volume 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; volume 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; volume 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.
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.
9780199722785 0199722781 1283252686 9781283252683
9786613252685
325268 MIL
Abnormalities, Human.
QM691 / .H65 2011
618.92/01
QS 675 / H751c 2011
Common malformations. - 1 online resource (481 pages)
Includes bibliographical references.
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; volume 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; volume 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; volume 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.
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.
9780199722785 0199722781 1283252686 9781283252683
9786613252685
325268 MIL
Abnormalities, Human.
QM691 / .H65 2011
618.92/01
QS 675 / H751c 2011