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Approximately 15%-20% of school-aged children suffer from mathematics learning difficulties (MLD). Most children with developmental dyscalculia (DD) or MLD also have comorbid cognitive deficits. Recent literature suggests that research should focus on uncovering the neural underpinnings of MLD across more inclusive samples, rather than limiting studies to pure cases of DD or MLD with highly stringent inclusion criteria. Therefore, this study aims to identify neural aberrancies that may be common across multiple MLD cases with different deficit profiles. Nine MLD cases and 45 typically developing (TD) children, all around 7 years old (27 boys), were recruited. Using functional near-infrared spectroscopy (fNIRS), brain data were collected during an approximate resting state and a mathematical computation task (addition). Graph theory was then applied to assess global and nodal network indicators of brain function. When comparing the network indicators and brain activation of the MLD cases to those of TD children, no unified neural aberrancy was found across all cases. However, three MLD cases did show distinct neural aberrancies compared to TD children. The study discusses the implications of these findings, considering both the neural aberrancies in the three MLD cases and the neural similarities found in the other six cases, which were comparable to those of the TD children. This raises important questions about the presence and nature of aberrant neural indicators in MLD across large cohorts and highlights the need for further research in this area.
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http://dx.doi.org/10.1111/ejn.16629 | DOI Listing |
Am J Cardiol
August 2025
Department of Cardiology, Peking University People's Hospital, 11 Xizhimen South Ave, Xicheng District, Beijing, 100044, China. Electronic address:
Myocardial bridging (MB) is a kind of congenital coronary abnormality. The functional impact of MB on coronary artery remains a subject of debate. This study aimed to assess the hemodynamic effects of MB using coronary angiography-derived fractional flow reserve (caFFR) and elucidate the relationship between MB anatomical parameters and diastolic caFFR (dcaFFR) in patients with isolated MB (iMB) and MB combined with proximal coronary atherosclerosis (MB+AS).
View Article and Find Full Text PDFPediatrics
August 2025
Nationwide Children's Hospital, Division of Primary Care Pediatrics.
Metachromatic leukodystrophy (MLD) is a lysosomal disorder affecting about 1 per 100,000 newborns. It is caused by biallelic variations in the arylsulfatase A (ARSA) gene, leading to deficiency of ARSA enzyme activity leading to elevation of sulfatides. Most affected individuals have the late-infantile or early-juvenile phenotype, associated with significant and progressive neurologic degeneration and death.
View Article and Find Full Text PDFZhonghua Nan Ke Xue
December 2024
Department of Urology, The 909th Hospital / Dongnan Hospital of Xiamen University, Zhangzhou, Fujian 363000, China.
Objective: To compare the effects of normal-pressure drainage (norPD) and negative-pressure drainage (negPD) after laparoscopic radical prostatectomy (LRP) in the treatment of PCa.
Methods: We retrospectively analyzed the clinical and follow-up data on 87 cases of PCa treated by LRP from October 2019 to October 2022, 46 receiving norPD and the other 41 negPD postoperatively. We indwelt an F20 pelvic drainage tube for each of the patients, which were connected to an anti-reflux drainage bag for those in the norPD group and a 200 ml negative pressure ball for those in the negPD group, and removed the tubes at the drainage volume ≤30 ml/d.
Beijing Da Xue Xue Bao Yi Xue Ban
August 2025
Department of General Surgery, Peking University Third Hospital, Beijing 100191, China.
Objective: To explore the safety of laparoscopic modified transcystic biliary drainage (modified C-tube technique) in the treatment of biliary stones and application of diagnosing biliary disease.
Methods: A retrospective analysis was conducted on the clinical data of 68 cases of biliary stones successfully treated with laparoscopic modified C-tube technique from August 2021 to December 2023. The safety, effectiveness, and area of applications were analyzed.
Brain Dev
July 2025
Department of Child Neurology, National Center of Neurology and Psychiatry, 4-1-1 Ogawahigashi-cho, Kodaira, Tokyo 187-8551, Japan. Electronic address:
We reviewed published articles on representative inherited cerebral white matter disorders that develop in childhood. In this paper, we described demyelinating disorders (adrenoleukodystrophy, globoid cell leukodystrophy or Krabbe disease, and metachromatic leukodystrophy), astrocytic disorders (Alexander disease and vanishing white matter disease), and disorders of water homeostasis in the myelin sheath (megalencephalic leukoencephalopathy with subcortical cysts and CLCN2-related leukoencephalopathy). The causes, symptoms, diagnostic imaging, and forefront of treatment for these disorders are discussed.
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