Zika Virus Infection
What's New
Last Posted: Jan 09, 2020
- Neurodevelopmental Abnormalities Associated With In Utero Zika Virus Infection in Infants and Children-The Unfolding Story.
Honein Margaret A et al. JAMA pediatrics 2020 Jan - Zika Birth Defects Surveillance
CDC, 2019 - Community Perspectives on Contraception in the Context of the Zika Virus in the U.S. Virgin Islands: Implications for Communication and Messaging.
Brittain Anna W et al. Women's health issues : official publication of the Jacobs Institute of Women's Health 2019 Mar - Identical Twins Hint at How Environments Change Gene Expression
Studying twins has long offered insight into the interplay of nature and nurture. Epigenetics is the next frontier. E Hayasaki, The Atlantic, May 2018 - Recognizing the Global Impact of Zika Virus Infection during Pregnancy.
Honein Margaret A et al. The New England journal of medicine 2018 Mar (11) 1055-1056 - Birth Defects Potentially Related to Zika Virus Infection During Pregnancy in the United States
B Fitzgerald et al, JAMA, Jan 25, 2018 - The genetics of congenitally small brains.
Duerinckx Sarah et al. Seminars in cell & developmental biology 2017 Sep - Health and Development at Age 19-24 Months of 19 Children Who Were Born with Microcephaly and Laboratory Evidence of Congenital Zika Virus Infection During the 2015 Zika Virus Outbreak - Brazil, 2017.
Satterfield-Nash Ashley et al. MMWR. Morbidity and mortality weekly report 2017 Dec (49) 1347-1351 - Update: Interim Guidance for the Diagnosis, Evaluation, and Management of Infants with Possible Congenital Zika Virus Infection - United States, October 2017.
Adebanjo Tolulope et al. MMWR. Morbidity and mortality weekly report 2017 Oct (41) 1089-1099 - Outcomes of Pregnancies with Laboratory Evidence of Possible Zika Virus Infection in the United States and the US Territories
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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
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