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1.
Zhonghua Liu Xing Bing Xue Za Zhi ; 44(5): 845-850, 2023 May 10.
Article de Chinois | MEDLINE | ID: mdl-37221077

RÉSUMÉ

Objective: To establish a dynamic syndromic surveillance system in the border areas of Yunnan Province based on information technology, evaluate its effectiveness and timeliness in the response to common communicable disease epidemics and improve the communicable disease prevention and control in border areas. Methods: Three border counties were selected for full coverage as study areas, and dynamic surveillance for 14 symptoms and 6 syndromes were conducted in medical institutions, the daily collection of information about students' school absence in primary schools and febrile illness in inbound people at border ports were conducted in these counties from January 2016 to February 2018 to establish an early warning system based on mobile phone and computer platform for a field experimental study. Results: With syndromes of rash, influenza-like illness and the numbers of primary school absence, the most common communicable disease events, such as hand foot and mouth disease, influenza and chickenpox, can be identified 1-5 days in advance by using EARS-3C and Kulldorff time-space scanning models with high sensitivity and specificity. The system is easy to use with strong security and feasibility. All the information and the warning alerts are released in the form of interactive charts and visual maps, which can facilitate the timely response. Conclusions: This system is highly effective and easy to operate in the detection of possible outbreaks of common communicable diseases in border areas in real time, so the timely and effective intervention can be conducted to reduce the risk of local and cross-border communicable disease outbreaks. It has practical application value.


Sujet(s)
Téléphones portables , Grippe humaine , Humains , Surveillance sentinelle , Syndrome , Chine
2.
Toxins (Basel) ; 13(11)2021 10 25.
Article de Anglais | MEDLINE | ID: mdl-34822539

RÉSUMÉ

It has long been accepted that Shiga toxin (Stx) only exists in Shigella dysenteriae serotype 1. However, in recent decades, the presence of Shiga toxin genes (stx) in other Shigella spp. have been reported. We screened 366 Shigella flexneri strains from Alberta, Canada (2003 to 2016) for stx and 26 positive strains were identified. These isolates are highly related with the majority originating from the Dominican Republic and three isolates with Haiti origin. Both phylogenetic and spanning tree analysis of the 26 Alberta and 29 stx positive S. flexneri originating from the U.S., France, Canada (Quebec) and Haiti suggests that there are geographic specific distribution patterns (Haiti and Dominican Republic clades). This study provides the first comprehensive whole genome based phylogenetic analysis of stx positive S. flexneri strains as well as their global transmission, which signify the public health risks of global spreading of these strains.


Sujet(s)
Maladies transmissibles importées/microbiologie , Dysenterie bacillaire/microbiologie , Shiga-toxine/génétique , Shigella dysenteriae/génétique , Alberta , République dominicaine , Haïti , Phylogenèse , Voyage , Séquençage du génome entier
3.
BMC Med Genet ; 20(1): 95, 2019 05 31.
Article de Anglais | MEDLINE | ID: mdl-31151415

RÉSUMÉ

BACKGROUND: Tubulinopathies result from mutations in tubulin genes, including TUBG1, responsible for cell microtubules, are characterized by brain development abnormalities, microcephaly, early-onset epilepsy, and motor impairment. Only eleven patients with TUBG1 mutations have been previously described in literature to our knowledge. Here we present two new patients with novel de novo TUBG1 mutations and review other cases in the literature. CASE PRESENTATIONS: Both patients have microcephaly and intellectual disability. Patient B further fits a more typical presentation, with well-controlled epilepsy and mild hypertonia, whereas Patient A's presentation is much milder without these other features. CONCLUSION: This report expands the spectrum of TUBG1 mutation manifestations, suggesting the possibility of less severe phenotypes for patients and families, and influencing genetic counselling strategies.


Sujet(s)
Prédisposition génétique à une maladie/génétique , Mutation faux-sens , Troubles du développement neurologique/génétique , Tubuline/génétique , Enfant , Femelle , Humains , Nourrisson , Mâle , Troubles du développement neurologique/anatomopathologie , Phénotype , Indice de gravité de la maladie
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