Genetics, Newborn Screening, and Inborn Errors of Metabolism, An Issue of Clinics in Perinatology
- 1 Edición, Volumen 52-3 - 27 de agosto de 2025
- Última edición
- Editores: Patrick K. Gallagher, Alex R. Kemper
- Idioma: Inglés
In this issue of Clinics in Perinatology, guest editors Drs. Patrick Gallagher and Alex R. Kemperbring their considerable expertise to the topic of Genetics, Newborn Screening… Leer más
Descripción
Descripción
In this issue of Clinics in Perinatology, guest editors Drs. Patrick Gallagher and Alex R. Kemperbring their considerable expertise to the topic of Genetics, Newborn Screening, and Inborn Errors of Metabolism. Early recognition through newborn screening is vital for detecting the 6,000 potentially affected newborns each year in the U.S., as timely treatment can prevent early death and long-term morbidity. In this issue, top experts provides important clinical updates in genetic testing, genome sequencing, and newborn screening.
Puntos claves
Puntos claves
- Contains 14 practice-oriented topics, including approach to the neonate with suspected inborn error of metabolism; prenatal genetic diagnosis; the future of clinical genomics; genetic testing in the neonate; genetics of congenital heart disease; and more
- Provides in-depth clinical reviews of genetics, newborn screening, and inborn errors of metabolism, offering actionable insights for clinical practice
- Presents the latest information on this timely, focused topic under the leadership of experienced editors in the field. Authors synthesize and distill the latest research and practice guidelines to create clinically significant, topic-based reviews
De interès para
De interès para
Perinatologists/Neonatologists
Índice
Índice
Newborn Screening: Advances, Challenges, and Future Directions
Newborn Screening for Hemoglobin Disorders
Cystic Fibrosis Newborn Screening
Newborn Screening of the Endocrine System: Best Practices for Evaluation of Hypothyroidism and Congenital Adrenal Hyperplasia
Early Hearing Detection
The Case for Universal Newborn Congenital Cytomegalovirus Screening
Newborn Pulse-Oximetry Screening
Prenatal Genetic Diagnosis: A Guide to Screening and Diagnostic Testing Options
Genetic Testing in the Neonate
Genetics of Congenital Heart Disease
The Emerging Role of Genome Sequencing in Newborn Screening
Newborn Screening for Hemoglobin Disorders
Cystic Fibrosis Newborn Screening
Newborn Screening of the Endocrine System: Best Practices for Evaluation of Hypothyroidism and Congenital Adrenal Hyperplasia
Early Hearing Detection
The Case for Universal Newborn Congenital Cytomegalovirus Screening
Newborn Pulse-Oximetry Screening
Prenatal Genetic Diagnosis: A Guide to Screening and Diagnostic Testing Options
Genetic Testing in the Neonate
Genetics of Congenital Heart Disease
The Emerging Role of Genome Sequencing in Newborn Screening
Detalles del producto
Detalles del producto
- Edición: 1
- Última edición
- Volumen: 52-3
- Publicado: 23 de septiembre de 2025
- Idioma: Inglés
Sobre los editores
Sobre los editores
PG
Patrick K. Gallagher
Afiliaciones y experiencia
Departments of Chemistry and Materials Science and Engineering, Columbus, Ohio, USAAK
Alex R. Kemper
Afiliaciones y experiencia
Division Chief of Primary Care Pediatrics Nationwide Childrens Hospital Professor of Pediatrics the Ohio State University College of Medicine Columbus, OH, USA