Results 61 to 70 of about 9,801 (176)

POLYMERASE CHAIN REACTION AND SEROLOGY TEST TO DETECT RUBELLA VIRUS IN CONGENITAL RUBELLA SYNDROME PATIENTS WITH HEARING LOSS

Indonesian Journal of Tropical and Infectious Disease, 2020
Rubella infections in pregnant women, especially during the first trimester, often lead to manifest as congenital rubella syndrome (CRS). This syndrome consists of several inherited disorders such as deafness, cataracts, and cardiac abnormalities ...
Sabrina Izzattisselim, Nyilo Purnami
doaj   +1 more source

Diagnostic Dilemma in an Infant With Sound‐Triggered Motor Events: Reflex Epilepsy Versus Exaggerated Startle—A Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Auditory‐triggered motor events in infancy present a significant diagnostic challenge due to overlap between epileptic and non‐epileptic startle phenomena. We report the case of a term female infant with neonatal‐onset seizures and subsequent development of reproducible sound‐triggered jerky movements, raising diagnostic uncertainty between ...
Aakash Pandit, Melisha Koirala, Anil Shahi, Anupama Sharma, Aashish Panta, Shuvra Rimal   +5 more
wiley   +1 more source

Clinical, Neuroimaging and Video Electroencephalography Findings in Children With Congenital Zika Syndrome: An Analysis From a Neurorehabilitation Centre

International Journal of Developmental Neuroscience, Volume 86, Issue 2, April 2026.
Children with congenital Zika syndrome followed at a neurorehabilitation centre demonstrated severe neurological impairment characterized by microcephaly, cortical malformations, intracranial calcifications and multifocal epileptiform activity. Integrated clinical, neuroimaging and video‐electroencephalographic (EEG) findings highlight the extensive ...
Adilina Soares Romeiro Rodrigues, Pedro Ykaro Fialho Silva, Ramiro Pinheiro Rodrigues, Kylvia Giselle Fernandes Dantas Pinho, Sthefani da Costa Penha, Álvaro Jorge Madeiro Leite   +5 more
wiley   +1 more source

CONGENITAL RUBELLA SYNDROME – CASE REPORT

Мать и дитя в Кузбассе, 2017
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, Татьяна Владимировна Зорькина, Александра Владимировна Богатырева, Ирина Владимировна Гребенкина, Владимир Владимирович Протопопов   +4 more
doaj  

Characteristics of Hearing Impairment in Patients with Suspected Congenital Rubella Syndrome at the ENT Clinic of Prof. Dr. I.G.N.G Ngoerah Hospital Denpasar, Indonesia

Journal of Community Medicine and Public Health Research
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, I Made Wiranadha   +1 more
doaj   +1 more source

Optimization and Validation of a Real Time Reverse Transcriptase Polymerase Chain Reaction with RNA Internal Control to Detect Rubella RNA

Indonesian Biomedical Journal, 2013
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

Factors Affecting Immune Reconstitution Post‐Allogeneic HSCT in Children: The Case for an Individualized Approach to Vaccination

European Journal of Haematology, Volume 116, Issue 4, Page 336-349, April 2026.
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, Frederic Baleydier, Laure Pittet, Geraldine Blanchard‐Rohner   +3 more
wiley   +1 more source

CONGENITAL RUBELLA SYNDROME

The Professional Medical Journal, 2006
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

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 642-652, March 2026.
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, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

Non‐Syndromic Paucity of Interlobular Bile Ducts (NSPIBD) Presenting as Neonatal Cholestasis in an Infant With Down Syndrome: A Case Report

Clinical Case Reports, Volume 14, Issue 3, March 2026.
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, Nurfirdaus Musa, Nurul Husna Mohd Dani, Zurina Zainuddin   +3 more
wiley   +1 more source