Buch, Englisch, 148 Seiten, Format (B × H): 161 mm x 241 mm, Gewicht: 286 g
Buch, Englisch, 148 Seiten, Format (B × H): 161 mm x 241 mm, Gewicht: 286 g
ISBN: 978-93-6616-693-3
Verlag: Jaypee Brothers Medical Publishers
Written in association with the Federation of Obstetric and Gynaecological Societies of India (FOGSI), and with contributions from a multitude of recognised experts led by FOGSI (2025-2026) president Sunita Tandulwadkar; the Ethical Evidence-based Recommendations (EEBR) series provides clinicians with the latest updates and advances in the field, with each book focusing on a different subspecialty.
As genetics becomes a more integral part of routine medical practice, it is essential that obstetricians, gynaecologists and other health care providers are aware of advances in the understanding of genetic disease and the fundamental principles of genetic screening and molecular testing. Prenatal genetic screenings and diagnostic tests provide information about the health of a foetus. It can help families and healthcare providers make decisions about a pregnancy or the foetus. Genetic tests check for congenital conditions like Down syndrome, trisomy 13 and spina bifida.
The EEBRs in this book begin with an explanation of conventional genetics and cytogenomics, followed by the basics of pedigree charting which diagrams the inheritance of a trait or health condition through generations of a family. The text goes on to discuss screening and testing, and a variety of common genetic disorders. The book concludes with a section on recent advances and research in the field.
Other titles in the series include:
- Antenatal Fetal Surveillance
- Endometriosis
- Fibroids
- Hyperglycemia in Pregnancy
- Hypertensive Disorders of Pregnancy
- Induction of Labor
- Polycystic Ovary Syndrome
- Postpartum Hemorrhage
- Preterm Labor
Autoren/Hrsg.
Weitere Infos & Material
1. Conventional Genetics and Cytogenomics
2. Basics of Pedigree Charting
3. Preconception Carrier Screening for Genetic Disorders
4. Ethical Considerations for Preconception Genetic Counseling in India
5. Prenatal Screening and Invasive Testing
6. Noninvasive Prenatal Testing Guidelines
7. Prenatal Genetic Evaluation of Fetal Anomalies
8. Fetal Autopsy and Placental Pathology
9. Approach to Intellectual Disability and/or Dysmorphism for Prenatal Diagnosis
10. Genetic of Recurrent Pregnancy Loss
11. Genetics and Hemoglobinopathies
12. Applications of Molecular Genetic Technologies to Prenatal Diagnosis
13. Preimplantation Genetic Testing: Key Questions, Recommendations, and Evidence Review
14. Cancer Genetics for Women
15. Research Advances and Future Directions in Obstetric Genetics
