Results 21 to 30 of about 10,526 (134)

RUBELLA VIRUS AND ITS TERATOGENIC ACTION. PATHOGENESIS, CLINICAL COURSE, DIAGNOSTICS AND PREVENTION OF CONGENITAL RUBELLA SYNDROME. ARTICLE 1. RUBELLA VIRUS: MOLECULAR–BIOLOGICAL CHARACTERISTICS

open access: yesИнфекция и иммунитет, 2014
. This review summarizes data about rubella virus and its teratogenic action, congenital rubella syndrome (CRS), modern methods of diagnostics and prevention of infection.
A. J. Antipova
doaj   +1 more source

Rubella IgM epidemiology in the pre-rubella vaccination era in Uganda

open access: yesBMC Infectious Diseases, 2020
Background Control of Rubella and Congenital Rubella Syndrome using vaccination has shown great success in the America’s. Uganda is due to introduce the Rubella vaccine however the magnitude of transmission is not well documented.
Fred Bagenda   +4 more
doaj   +1 more source

Congenital rubella syndrome and anesthetic considerations

open access: yesMRIMS Journal of Health Sciences, 2018
Blindness in infants due to congenital cataract is up to 5-20% of all the vision loss of which 25% is due to Congenital Rubella Syndrome (CRS). CRS is a constellation of multi-system abnormalities with each posing its own variant of anesthetic dilemmas ...
Manjula V Ramsali   +3 more
doaj   +1 more source

Rubella Vaccine Introduction in the South African Public Vaccination Schedule: Mathematical Modelling for Decision Making

open access: yesVaccines, 2020
Background: age structured mathematical models have been used to evaluate the impact of rubella-containing vaccine (RCV) introduction into existing measles vaccination programs in several countries. South Africa has a well-established measles vaccination
Nkengafac Villyen Motaze   +4 more
doaj   +1 more source

Case based rubella surveillance in Abia State, South East Nigeria, 2007–2011 [PDF]

open access: yesPeerJ, 2014
Introduction. Rubella infection has the potential of causing severe fetal birth defects collectively called congenital rubella syndrome (CRS) if the mother is infected early in pregnancy.
Chukwuemeka Anthony Umeh   +1 more
doaj   +2 more sources

TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non‐Syndromic Hearing Loss

open access: yesAdvanced Science, EarlyView.
TECTB is a non‐collagenous protein of the tectorial membrane – an extracellular matrix of the cochlea. This study identifies dominant missense variants in TECTB linked to human hereditary deafness in two unrelated families. Genetically engineered mice homozygous for one of the variants are profoundly deaf, whereas heterozygous mice have normal hearing ...
Evan B. Hale   +23 more
wiley   +1 more source

The status of rubella IgG antibody titer between antenatal and postnatal among pregnant non-immune to rubella

open access: yesHuman Vaccines & Immunotherapeutics, 2021
Background: The infection of rubella in pregnancy is worrisome due to the fact that it causes miscarriages, congenital defects, and Congenital Rubella Syndrome (CRS).
Irfana Rasool   +4 more
doaj   +1 more source

First Report of Uniparental Isodisomy of Chromosome 15 Revealing Angelman Syndrome and Microphthalmia Associated With a Novel Homozygous ALDH1A3 Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Paternal isodisomy of chromosome 15 (iUPD15) is a recognized cause of Angelman syndrome (AS), accounting for approximately 2%–5% of cases. Additionally, another recognized consequence of iUPD is the unmasking of autosomal recessive disorders. However, reports of recessive disorders resulting from iUPD15 remain scarce in the literature.
Gabriela Roldão Correia‐Costa   +4 more
wiley   +1 more source

Congenital rubella syndrome and its protean manifestation in Nigeria

open access: yesEgyptian Pediatric Association Gazette
Background Congenital rubella syndrome (CRS) arises from intrauterine infections with the rubella virus especially during the first trimester of pregnancy. It affects various systems resulting in disastrous outcomes.
Nubwa Yusufu Papka   +4 more
doaj   +1 more source

Prenatal Detection of Arthrogryposis Multiplex Congenita, Present State and Future Perspectives

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is a heterogeneous group of conditions characterized by congenital contractures in at least two different body regions. Despite increasingly widespread prenatal ultrasound screening, prenatal detection rates for AMC remain disappointingly low, with fewer than half of affected fetuses diagnosed before ...
Arda Arduç   +14 more
wiley   +1 more source

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