Results 61 to 70 of about 9,801 (180)
CONGENITAL RUBELLA SYNDROME – CASE REPORT
Case report had devoted to clinical observation and diagnistical process of congenital rubella syndrome (CRD) on newborn gerl. The presentation of congenital rubella syndrome consist the brain defect,nervus opticis atrophy,hearing impartment, vision ...
Мария Константиновна Соболева +4 more
doaj
Asymptomatic rubella virus infection can cause delays in the diagnosis of rubella in pregnant women, leading to the development of congenital rubella syndrome (CRS). The clinical manifestations of congenital rubella syndrome are called the rubella triad,
I Gede Wahyu Adi Raditya +1 more
doaj +1 more source
BACKGROUND: According to a report from WHO, cases of rubella infection in Indonesia has increased up to 10-fold from 2007 to 2011. Despite no data of congenital rubella syndrome in the report, there are approximately 45,000 cases of babies born with ...
Winny Xie, Yusmiati Yusmiati
doaj +1 more source
ABSTRACT Allogeneic hematopoietic stem cell transplantation (HSCT) is increasingly used to treat malignant and non‐malignant diseases. Following allogeneic HSCT, patients are particularly vulnerable to vaccine‐preventable diseases (VPD) because conditioning depletes immune cells, including memory cells.
Hélène Buvelot +3 more
wiley +1 more source
Rubella is a major public health problem which is usually a mild rashillness in children and adults. However, its seriousness and public health importance stems from the ability of Rubellavirus to cross the placental barrier and infect fetal tissue, which may result in congenital rubella syndrome. Themechanism by which Rubella virus causes fetal damage
openaire +2 more sources
Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää +14 more
wiley +1 more source
A case of congenital rubella syndrome and epidemiology of related cases in China, 2014–2023
Rubella is a major cause of congenital defects, and the presence of rubella infection in a pregnant woman may lead to fetal death or congenital defects known as congenital rubella syndrome(CRS).
Xiaoying Gong +4 more
doaj +1 more source
ABSTRACT Non‐syndromic paucity of interlobular bile ducts (NSPIBD) is a rare cause of neonatal cholestasis, often presenting with clinical features similar to extrahepatic biliary atresia. This report presents a case of NSPIBD in an infant with Down syndrome who exhibited jaundice and pale stools.
Pui Ling Thong +3 more
wiley +1 more source
Prevalence of rubella-specific IgG antibodies in unimmunized young female population
Context: Rubella is a mild self-limiting disease all over the world; nevertheless, it is of significant public health importance due to its teratogenic effect of congenital rubella syndrome.
Jayakrishnan Thayyil +4 more
doaj +1 more source
Immunoglobulin products derived from pooled global plasma reflect population‐level antiviral immunity. Analysis of batches from 2017 to 2023 reveals pandemic‐driven shifts in viral antibody profiles and a concurrent rise in autoantibodies, notably against TRIM21/Ro52, highlighting links between SARS‐CoV‐2, immunity debt, and autoimmunity.
Hannes Lindahl +4 more
wiley +1 more source

