Non-Invasive Prenatal Screening of Rare Fetal Genetic Diseases
eBook - ePub

Non-Invasive Prenatal Screening of Rare Fetal Genetic Diseases

  1. 221 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Non-Invasive Prenatal Screening of Rare Fetal Genetic Diseases

About this book

Non-Invasive Prenatal Screening of Rare Fetal Genetic Diseases offers a comprehensive exploration of the latest advancements in non-invasive prenatal screening (NIPS) technologies and their application in detecting rare fetal genetic disorders. It provides a detailed overview of current methods in NIPS technology, the application of NIPS in detecting rare genetic disorders, and ethical considerations. Sections cover advanced genomic methods such as Next-Generation Sequencing, Single-Nucleotide Polymorphism analysis, and Comparative Genomic Hybridization, highlighting their impact on the accuracy and scope of NIPS, while also exploring specific genetic disorders, including Trisomy 18, Trisomy 13, Duchenne Muscular Dystrophy, Angelman Syndrome, Turner Syndrome, and Cri du Chat Syndrome.Researchers will find this to be a valuable resource for understanding and applying NIPS protocols in their work, while clinicians will benefit from practical insights on appropriate screening methods, interpreting NIPS results, and counseling expectant parents. This book is an essential resource for researchers in obstetrics and gynecology, genetic counselors, and professionals in the biotechnology and pharmaceutical industries. It equips readers with the knowledge and tools needed to advance their work and improve prenatal care practices. - Provides a comprehensive overview of advancements in NIPS technology for detecting rare fetal genetic disorders - Discusses emerging trends, potential challenges, and ethical considerations in the application of NIPS - Highlights practical insights and research findings that enhance prenatal care and screening methods - Explores the integration of advanced genomic methods in NIPS, including Next-Generation Sequencing and SNP analysis - Offers case studies and clinical examples to illustrate the practical application of NIPS in prenatal screening

Information

Publisher
Academic Press
Year
2026
Topic
Biological Sciences
eBook ISBN
9780443276613
Subtopic
Genetics & Genomics
Index
Biological Sciences

Table of contents

  1. Title of Book
  2. Chapter 1. Introduction to rare genetic diseases in fetal development
  3. Chapter 2. Emergence of non-invasive prenatal screening in clinical practice
  4. Chapter 3. Advanced genomic methods in non-invasive prenatal screening
  5. Chapter 4. Trisomy disorders: trisomy 21 (Down's syndrome), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13)
  6. Chapter 5. Sex chromosome aneuploidies: Klinefelter syndrome, triple X syndrome, and monosomy X (turner syndrome)
  7. Chapter 6. Neurodevelopmental disorders: Angelman Syndrome & Duchenne Muscular Dystrophy
  8. Chapter 7. Chromosomal deletion syndromes: DiGeorge syndrome and cri du chat syndrome
  9. Chapter 8. Rare metabolic disorders: Alagille syndrome and hypophosphatasia
  10. Chapter 9. Genetic disorders affecting growth and development: Prader–Willi syndrome and neurofibromatosis type 1
  11. Chapter 10. Ethical considerations in non-invasive prenatal screening
  12. Index

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Yes, you can access Non-Invasive Prenatal Screening of Rare Fetal Genetic Diseases by Riyaz Ahmad Rather in PDF and/or ePUB format, as well as other popular books in Biological Sciences & Genetics & Genomics. We have over 1.5 million books available in our catalogue for you to explore.