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...
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1. Verfasser: | |
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Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
Oxford :
Oxford University Press, USA,
2011.
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Schlagworte: | |
Online-Zugang: | Volltext |
Zusammenfassung: | 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. |
Beschreibung: | 1 online resource (481 pages) |
Bibliographie: | Includes bibliographical references. |
ISBN: | 9780199722785 0199722781 1283252686 9781283252683 |
Internformat
MARC
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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. | |
650 | 0 | |a Abnormalities, Human. |0 http://id.loc.gov/authorities/subjects/sh85000182 | |
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Datensatz im Suchindex
DE-BY-FWS_katkey | ZDB-4-EBA-ocn751694637 |
---|---|
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adam_text | |
any_adam_object | |
author | Holmes, Lewis B. |
author_facet | Holmes, Lewis B. |
author_role | |
author_sort | Holmes, Lewis B. |
author_variant | l b h lb lbh |
building | Verbundindex |
bvnumber | localFWS |
callnumber-first | Q - Science |
callnumber-label | QM691 |
callnumber-raw | QM691 .H65 2011 |
callnumber-search | QM691 .H65 2011 |
callnumber-sort | QM 3691 H65 42011 |
callnumber-subject | QM - Human Anatomy |
collection | ZDB-4-EBA |
contents | 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. |
ctrlnum | (OCoLC)751694637 |
dewey-full | 618.92/01 |
dewey-hundreds | 600 - Technology (Applied sciences) |
dewey-ones | 618 - Gynecology, obstetrics, pediatrics, geriatrics |
dewey-raw | 618.92/01 |
dewey-search | 618.92/01 |
dewey-sort | 3618.92 11 |
dewey-tens | 610 - Medicine and health |
discipline | Medizin |
format | Electronic eBook |
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id | ZDB-4-EBA-ocn751694637 |
illustrated | Not Illustrated |
indexdate | 2024-11-27T13:17:59Z |
institution | BVB |
isbn | 9780199722785 0199722781 1283252686 9781283252683 |
language | English |
oclc_num | 751694637 |
open_access_boolean | |
owner | MAIN DE-863 DE-BY-FWS |
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physical | 1 online resource (481 pages) |
psigel | ZDB-4-EBA |
publishDate | 2011 |
publishDateSearch | 2011 |
publishDateSort | 2011 |
publisher | Oxford University Press, USA, |
record_format | marc |
spelling | Holmes, Lewis B. Common malformations. Oxford : Oxford University Press, USA, 2011. 1 online resource (481 pages) text txt rdacontent computer c rdamedia online resource cr rdacarrier 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. Includes bibliographical references. Print version record. 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. Abnormalities, Human. http://id.loc.gov/authorities/subjects/sh85000182 Congenital Abnormalities Malformations. MEDICAL Nursing Pediatric & Neonatal. bisacsh MEDICAL Perinatology & Neonatology. bisacsh Abnormalities, Human fast has work: Common malformations (Text) https://id.oclc.org/worldcat/entity/E39PCFHkY8rrRPxcgvb6pqm9Tb https://id.oclc.org/worldcat/ontology/hasWork Print version: 9780195136029 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=389271 Volltext |
spellingShingle | Holmes, Lewis B. Common malformations. 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. Abnormalities, Human. http://id.loc.gov/authorities/subjects/sh85000182 Congenital Abnormalities Malformations. MEDICAL Nursing Pediatric & Neonatal. bisacsh MEDICAL Perinatology & Neonatology. bisacsh Abnormalities, Human fast |
subject_GND | http://id.loc.gov/authorities/subjects/sh85000182 |
title | Common malformations. |
title_auth | Common malformations. |
title_exact_search | Common malformations. |
title_full | Common malformations. |
title_fullStr | Common malformations. |
title_full_unstemmed | Common malformations. |
title_short | Common malformations. |
title_sort | common malformations |
topic | Abnormalities, Human. http://id.loc.gov/authorities/subjects/sh85000182 Congenital Abnormalities Malformations. MEDICAL Nursing Pediatric & Neonatal. bisacsh MEDICAL Perinatology & Neonatology. bisacsh Abnormalities, Human fast |
topic_facet | Abnormalities, Human. Congenital Abnormalities Malformations. MEDICAL Nursing Pediatric & Neonatal. MEDICAL Perinatology & Neonatology. Abnormalities, Human |
url | https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=389271 |
work_keys_str_mv | AT holmeslewisb commonmalformations |