Hearing loss
What's New
Last Posted: Sep 29, 2022
- GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss.
Melidis Damianos P et al. PLoS computational biology 2022 18(9) e1009785 - The Frequency of Common Deafness-Associated Variants Among 3,555,336 Newborns in China and 141,456 Individuals Across Seven Populations Worldwide.
Zhang Jiao et al. Ear and hearing 2022 - Congenital hearing loss: a literature review of the genetic etiology in a Mexican population.
Torre-González Carlos de la et al. Boletin medico del Hospital Infantil de Mexico 2022 79(4) 206-214 - Achondroplasia in Latin America: practical recommendations for the multidisciplinary care of pediatric patients.
Llerena Juan et al. BMC pediatrics 2022 22(1) 492 - Association Between Expanded Genomic Sequencing Combined With Hearing Screening and Detection of Hearing Loss Among Newborns in a Neonatal Intensive Care Unit.
Zhu Yunqian et al. JAMA network open 2022 5(7) e2220986 - Comprehensive Genomic Sequencing-Based Screening for Hearing Loss in the Neonatal Intensive Care Setting-Is It Time?
Abou Tayoun Ahmad N et al. JAMA network open 2022 5(7) e2220992 - The Impact of COVID-19 on Universal Newborn Hearing Screening.
Gallus Roberto et al. Ear and hearing 2022 - Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Li Marilyn M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022 24(7) 1392-1406 - Comprehensive Genomic Sequencing–Based Screening for Hearing Loss in the Neonatal Intensive Care Setting—Is It Time?
AN Abou Tayoun, JAMA Network Open, July 11, 2022 - Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation.
Elander Johanna et al. International journal of pediatric otorhinolaryngology 2022 159111218
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About RCH PHGKB
Reproductive and Child Health PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to reproductive and child Health...more
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- CDC Publications (1)
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- Ethical/Legal and Social Issues (ELSI) (4)
Common RCH Related Topics
- Attention Deficit/Hyperactivity Disorder
- Autism
- Birth Defects
- Carrier Testing
- Cerebral Palsy
- Congenital heart defects
- Pregnancy loss
- Developmental Disabilities
- Gestational Diabetes
- Hearing loss
- Neural tube defects
- Infant Mortality
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- Learning disability
- Newborn Screening
- Preeclampsia
- Prematurity
- Prenatal Testing
- Stillbirth
- Sudden Infant Death Syndrome
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Jul 25, 2022
- Page last updated:Oct 01, 2022
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