We report the first case of intrafamily transmission of a C-MRSA clone harbouring toxic shock syndrome toxin-1 (TSST-1). Because of the risk of this clone to spread in the community, family members of these patients should be screened to detect and prevent the diffusion of recurrent or new infections.
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http://dx.doi.org/10.1080/00365540701827499 | DOI Listing |
Leg Med (Tokyo)
December 2024
Institut de Médecine Légale, IML/UMJ, CHU Poitiers, rue de la Milétrie, CS 90577, 86021 POITIERS Cedex, France; Faculté de Médecine et de Pharmacie, Univ Poitiers, 6 rue de la Milétrie, 86073 Poitiers, France; Unité de Recherche Clinique, Centre Hospitalier Henri-Laborit, 370 av Jacques Cœur, 86000 Poitiers, France. Electronic address:
In the past several years, children and adolescents have increasingly been enticed into playing dangerous and challenging games, particularly through social networks. Epidemiological data regarding this phenomenon are particularly difficult to come by, as is information regarding the somatic and psychological consequences of these activities, which can end up having fatal outcomes. We here report the case of a suspicion of child abuse that turned out to be due to participation in a challenge game known as "The Deodorant Challenge" by a 10-year-old child who presented with burn-like lesions.
View Article and Find Full Text PDFPediatr Rheumatol Online J
December 2024
Translational Genetics Research Group, La Fe Health Research Institute (IIS La Fe), Avenida Fernando Abril Martorell nº 106 Tower A, 7th Floor, Valencia, Spain.
Background: Aicardi-Goutières Syndrome is a monogenic type 1 interferonopathy with infantile onset, characterized by a variable degree of neurological damage. Approximately 7% of Aicardi-Goutières Syndrome cases are caused by pathogenic variants in the ADAR gene and are classified as Aicardi-Goutières Syndrome type 6. Here, we present a new homozygous pathogenic variant in the ADAR gene.
View Article and Find Full Text PDFBMJ Case Rep
December 2024
Ophthalmology, Penn State College of Medicine, Hershey, Pennsylvania, USA.
Bardet-Biedl syndrome (BBS), an autosomal recessive ciliopathy with pleiotropic effects, manifests as a spectrum of anomalies involving multiple genes and affects fewer than 3,000 individuals in the USA. Due to its rarity and phenotypic variability, early diagnosis of BBS poses a significant challenge. Therefore, we aim to shed light on the intrafamilial phenotypic variation of BBS resulting from a variant by delineating the clinical presentation in two siblings.
View Article and Find Full Text PDFEur J Pediatr
December 2024
University Children's Hospital, Katholisches Klinikum Bochum, Ruhr-University Bochum, 44791, Bochum, Germany.
Unlabelled: In 2022, over 1,000,000 people from Ukraine fled to Germany, mostly women and children. The aim of this study was to determine health status and socio-demographic background of Ukrainian refugee minors in Germany and to compare that to German minors. In this study, Ukrainian refugees of all ages, who voluntarily made contact with the study centres via flyers or refugee shelters, were interviewed with the help of trained interpreters from 09-12/2022.
View Article and Find Full Text PDFCureus
October 2024
Ophthalmology, University of Arkansas for Medical Sciences, Little Rock, USA.
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