Hearing loss
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Last Posted: Jun 06, 2024
- Etiology of Childhood Profound Sensorineural Hearing Loss: The Role of Hearing Loss Gene Panel Testing.
Kaukab Rajput et al. Otolaryngol Head Neck Surg 2024 - Clinical characteristics and hearing loss etiology of cochlear implantees undergoing surgery in their teens, 20s, and 30s.
Goun Choe et al. Eur Arch Otorhinolaryngol 2024 - Rethinking non-syndromic hearing loss and its mimics in the genomic era
B Vona, EJHG, March 6, 2024 - Leading Risk Factors for Congenital Deafness in the Context of Universal Neonatal Screening: Our Observations in a Four-Year Retrospective Study.
Antoine Paul et al. Int J Neonatal Screen 2024 10(1) - Deaf boy can now hear after breakthrough gene treatment
Medical XPress, January 23, 2024 - Evaluation of newborn hearing screening results of infants with phenylketonuria.
Fatih Yüksel et al. Int J Pediatr Otorhinolaryngol 2024 177111840 - Genetics evaluation outcomes of patients with pediatric hearing loss: 2008-2022 retrospective study.
Sarah Mazzola et al. Am J Otolaryngol 2023 45(2) 104196 - A cost-effectiveness analysis of pre-pregnancy genetic screening for deafness: an empirical study in China.
Yipeng Lv et al. Front Public Health 2023 111081339 - Carrier screening for present disease prevalence and recessive genetic disorder in Taiwanese population.
Li Shan Chen et al. J Hum Genet 2023 - Next-generation sequencing for genetic testing of hearing loss populations.
Lulu Wang et al. Clin Chim Acta 2023 552117693
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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
Content Summary
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
- Infertility
- 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 Public Health Genomics Branch 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:Feb 1, 2024
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