Congenital Cytomegalovirus
What's New
Last Posted: May 08, 2023
- Genetic Underpinnings and Audiological Characteristics in Children With Unilateral Sensorineural Hearing Loss.
Chen-Yu Lee, et al. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2023 0 - Distribution of CMV envelope glycoprotein B, H and N genotypes in infants with congenital cytomegalovirus symptomatic infection.
Dong Niuniu, et al. Frontiers in pediatrics 2023 0 1112645 - Association between single nucleotide polymorphisms (SNPs) of IL1, IL12, IL28 and TLR4 and symptoms of congenital cytomegalovirus infection.
Jedli?ska-Pijanowska Dominika, et al. PloS one 2020 0 (5) e0233096 - Executive Functions, Pragmatic Skills, and Mental Health in Children With Congenital Cytomegalovirus (CMV) Infection With Cochlear Implants: A Pilot Study.
Löfkvist Ulrika, et al. Frontiers in psychology 2020 0 2808 - The Limitations of Cytomegalovirus DNA Detection in Cerebrospinal Fluid of Newborn Infants With Congenital CMV Infection: A Tertiary Care Neonatal Center Experience.
Czech-Kowalska Justyna, et al. The Pediatric infectious disease journal 2021 0 (9) 838-845 - HLA-E restricted cytomegalovirus UL40 peptide polymorphism may represent a risk factor following congenital infection.
Tarragó David, et al. BMC genomics 2022 0 (1) 455 - Cytomegalovirus variation among newborns treated with valganciclovir.
Dobbins G Clement, et al. Antiviral research 2022 0 105326 - Congenital Cytomegalovirus Infection and Permanent Hearing Loss in Rural North Indian Children.
Dar Lalit, et al. The Pediatric infectious disease journal 2016 0 (7) 670-673 - Congenital Cytomegalovirus Infection: Maternal-Child HLA-C, HLA-E, and HLA-G Affect Clinical Outcome.
Rovito Roberta, et al. Frontiers in immunology 2018 0 1904 - Single Nucleotide Polymorphisms of Interleukins and Toll-like Receptors and Neuroimaging Results in Newborns with Congenital HCMV Infection.
Czech-Kowalska Justyna, et al. Viruses 2021 9 (9) - Association between single nucleotide polymorphisms and viral load in congenital cytomegalovirus infection.
Jedli?ska-Pijanowska Dominika, et al. Journal of mother and child 2021 1 - Association of toll-like receptors polymorphism and intrauterine transmission of cytomegalovirus.
Eldar-Yedidia Yifat, et al. PloS one 2017 0 (12) e0189921 - A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children.
Shearer A Eliot et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Jun - National Cytomegalovirus (CMV) Awareness Month
CDC, June 2019 - Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children.
Boudewyns An et al. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2018 Jul 39(6) 732-738 - Maternal and child human leukocyte antigens in congenital cytomegalovirus infection.
Rovito Roberta, et al. Journal of reproductive immunology 2018 1 39-45 - Cytokine gene polymorphism associations with congenital cytomegalovirus infection and sensorineural hearing loss.
Kasztelewicz B, et al. European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology 2017 5 - Comparison of the Motor Performance and Vestibular Function in Infants with a Congenital Cytomegalovirus Infection or a Connexin 26 Mutation: A Preliminary Study.
Maes Leen, et al. Ear and hearing 2016 8 - A Thr72Ala polymorphism in the NKG2D gene is associated with early symptomatic congenital cytomegalovirus disease.
Taniguchi Rumi et al. Infection 2015 Jun (3) 353-9 - Does congenital cytomegalovirus infection lead to hearing loss by inducing mutation of the GJB2 gene?
Li Lu-Quan, et al. Pediatric research 2013 8 (2) 121-6 - Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patients.
Teek R, et al. Advances in medical sciences 2013 0 (2) 419-28 - Polymorphisms in TLR-2 are associated with congenital cytomegalovirus (CMV) infection but not with congenital CMV disease.
Taniguchi R, et al. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 2013 7 - Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccine.
Arav-Boger Ravit, et al. BMC research notes 2012 0 (1) 140 - [Audiologic and molecular screening for hearing loss by 35delG mutation in connexin 26 gene and congenital cytomegalovirus infection].
Streitenberger Edgardo Raúl, et al. Archivos argentinos de pediatría 2011 12 (6) 479-84 - Congenital cytomegalovirus
From NCATS Genetic and Rare Diseases Information Center - Sensorineural hearing loss in a pediatric population: association of congenital cytomegalovirus infection with intracranial abnormalities.
Kimani Jane W, et al. Archives of otolaryngology--head & neck surgery 2010 10 (10) 999-1004 - GJB2 and GJB6 mutations in children with congenital cytomegalovirus infection.
Ross Shannon A, et al. Pediatric research 2007 6 (6) 687-91
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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
- Content source: