Hearing loss
What's New
Last Posted: Sep 23, 2021
- Enzyme replacement therapy with galsulfase for mucopolysaccharidosis type VI.
Brunelli Marcela Junqueira et al. The Cochrane database of systematic reviews 2021 9CD009806 - Universal newborn hearing screening in the Italian Region of Sicily in 2018.
Ferlito Salvatore et al. Acta otorhinolaryngologica Italica : organo ufficiale della Societa italiana di otorinolaringologia e chirurgia cervico-facciale 2021 41(4) 356-363 - Osteogenesis Imperfecta and hearing loss in the paediatric population.
Joseph Judith K et al. International journal of pediatric otorhinolaryngology 2021 150110914 - Knowledge, attitude and management of hearing screening in children among family physicians in the Kingdom of Saudi Arabia.
Alqudah Ola et al. PloS one 2021 16(8) e0256647 - VIP-HL: Semi-automated ACMG/AMP variant interpretation platform for genetic hearing loss.
Peng Jiguang et al. Human mutation 2021 - Detecting Hearing Loss in Infants With a Syndrome or Craniofacial Abnormalities Following the Newborn Hearing Screen.
Horn Philippa et al. Journal of speech, language, and hearing research : JSLHR 2021 1-9 - Audiologists' perspectives on management of mild bilateral hearing loss in infants and young children.
Ching Teresa Y C et al. International journal of audiology 2021 1-9 - First glance at the molecular etiology of hearing loss in French-Canadian families from Saguenay-Lac-Saint-Jean's founder population.
Cruz Marino Tania et al. Human genetics 2021 - Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A).
Iannaccone Alessandro et al. American journal of medical genetics. Part A 2021 - A Genome-First Approach to Rare Variants in Dominant Postlingual Hearing Loss Genes in a Large Adult Population.
Ahmadmehrabi Shadi et al. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2021 1945998211029544
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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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- State Public Health Genomics Programs (29)
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- Tools/Methods (6)
- Ethical/Legal and Social Issues (ELSI) (4)
Common RCH Related Topics
- Attention Deficit/Hyperactivity Disorder
- Autism
- Birth Defects
- Carrier Testing
- Cerebral Palsy
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- 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:Oct 1, 2021
- Page last updated:Oct 22, 2021
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