• Zamawiaj do paczkomatu
  • Płać wygodnie
  • Obniżka
Genetic Consultations in the Newborn

Genetic Consultations in the Newborn

9780199990993
Print on demand. This item has an extended shipping time. The typical delivery time is 4-8 weeks.
702,00 zł
631,80 zł Zniżka 70,20 zł Brutto
Najniższa cena w okresie 30 dni przed promocją: 631,80 zł
Ilość
Od 4 do 6 tygodni

  Dostawa

Wybierz Paczkomat Inpost, Orlen Paczkę, DPD, Pocztę, email (dla ebooków). Kliknij po więcej

  Płatność

Zapłać szybkim przelewem, kartą płatniczą lub za pobraniem. Kliknij po więcej szczegółów

  Zwroty

Jeżeli jesteś konsumentem możesz zwrócić towar w ciągu 14 dni*. Kliknij po więcej szczegółów

Opis
The definitive work in genetic evaluation of newborns. I cannot recommend it strongly enough. -Judith G. HallAs demand continues to exceed availability when it comes to clinical geneticists, Genetic Consultations in the Newborn offers an essential new resource for practitioners everywhere:: a streamlined diagnostic manual that connects subtle symptoms of newborn dysmorphology to their differential diagnosis. Comprising more than 60 chapters organized by system and symptom, this book facilitates fast, expert navigation from recognition to management in syndromes that manifest during the newborn period. Richly illustrated and packed with pearls of practical wisdom from the authors decades of practice, it empowers readers to recognize the outward signs and symptoms crucial for an effective diagnosis. For geneticists, neonatologists, pediatricians, and anyone else who cares for infants in their first days of life, Genetic Consultations in the Newborn provides an essential and unmatched resource for navigating one of the most challenging areas of clinical practice. It should not be missed.
Szczegóły produktu
OUP USA
88321
9780199990993
9780199990993

Opis

Rok wydania
2019
Numer wydania
1
Oprawa
twarda
Liczba stron
400
Wymiary (mm)
216 x 279
Waga (g)
1500
  • Common issues in the newborn ; 1. Hypotonia; 2. Intrauterine growth retardation; 3. Overgrowth; 4. Twins; 5. Non-Immune hydrops; 6. Teratogenic agents; Cardiovascular System ; 7. Cardiac defects; 8. Heterotaxy; Craniofacial Sysyem; 9. Ear anomalies; 10. Eye anomalies; 11. Cleft lip; 12. Cleft palate; 13. Craniosynostoses; Central Nervous System; ; 14. Macrocephaly; 15. Microcephaly; 16. Cerebellar malformations; 17. Holoprosencephaly; 18. Hydrocephalus; 19. Neural tube defects; 20. Perinatal stroke; Gastrointestinal System; ; 21. Diaphragmatic hernia; 22. Gastroschisis; 23. Omphalocele; 24. Anorectal malformations; 25. Hirschsprung disease; Genitourinary System ; 26. Renal anomalies; 27. Hypospadias; Skeletal System; ; Limbs; 28. Arthrogryposis; 29. Club foot; 30. Upper extremity anomalies; 31. Lower extremity anomalies; 32. Polydactyly; 33. Syndactyly; Skeletal Dysplasias; 34. Skeletal dysplasias: Overview; 35. Skeletal dysplasias: Life limiting; 36. Skeletal dysplasias: Viable; 37. Fractures; Skin System; 38. Skin: Ectodermal dysplasias; 39. Skin: Epidermolysis bullosa; 40. Skin: Ichthyoses; 41. Skin: Vascular malformations; 42. Skin: Other disorders; Syndromes that commonly present in the newborn ; 1s. Trisomy 21; 2s. Trisomy 18; 3s. Trisomy 13; 4s. Turner syndrome; 5s. Wolf-Hirschhorn syndrome; 6s. Chr 5p minus syndrome; 7s. Deletion Chr 22q11.2; 8s. Achondroplasia; 9s. Beckwith Wiedemann syndrome; 10s. CHARGE syndrome; 11s. Cornelia de Lange syndrome; 12s. Diabetic Embryopathy; 13s. Fetal Alcohol Spectrum disorder; 14s. Incontinentia pigmenti; 15s. Prader Willi syndrome; 16s. Noonan syndrome; 17s. Smith Lemli Opitz syndrome; 18s. VATER/VACTERL association; 19s. Williams syndrome;
Komentarze (0)