Publications by authors named "Chen Mingren"

Article Synopsis
  • Kabuki syndrome (KS) is a rare genetic disorder marked by unique facial characteristics, intellectual disability, and various congenital anomalies, studied in a group of 23 Taiwanese patients.
  • Genetic analysis revealed that 22 patients had mutations, predominantly missense, nonsense, and frameshift variants, while one had a variant with uncertain significance.
  • Common clinical features included distinctive facial traits (100%), intellectual disability (100%), and development delays, with other issues such as heart abnormalities and seizures being noted, emphasizing the necessity of genetic testing and multidisciplinary approaches for proper diagnosis and management.
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Congenital heart defects (CHDs) affect a substantial proportion of patients with Kabuki syndrome. However, the prevalence and type of CHD and the genotype-phenotype correlations in Asian populations are not fully elucidated. This study performed a retrospective analysis of 23 Taiwanese patients with molecularly confirmed Kabuki syndrome.

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BACKGROUND An aortopulmonary window (APW) is an uncommon congenital defect of the septation between the ascending aorta and pulmonary trunk. The combination of APW and interrupted aortic arch (IAA) is even rarer, with the hallmark characteristics of high peri-operative mortality and postoperative obstruction of the aortic arch, pulmonary artery, and left main bronchus. These complications often need re-interventions.

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22q11.2 deletion syndrome (22q11.2DS) is a microdeletion syndrome exhibiting significant clinical phenotype variability.

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BACKGROUND Kawasaki disease (KD), a systemic vasculitis, affects children aged <5 years and is the leading acquired cardiovascular disease in developed countries. Although intravenous immunoglobulin is an effective treatment for KD and decreases the rate of cardiovascular complications, some patients still develop coronary sequelae, including coronary aneurysms and myocardial infarction. CASE REPORT A 9-year-old boy was diagnosed with KD at the age of 6 years.

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We investigated the hemodynamic parameters of pediatric PDA patients and focused on the influence of PDA size on pulmonary arterial pressure and the prevalence of pulmonary hypertension. A total of 52 patients aged between 2 months and 20 years who received transcatheter closure of a PDA from January 2018 to June 2022 in our institution were retrospectively recruited. Their hemodynamic parameters collected both by echocardiography and by cardiac catheterization were analyzed to delineate the influence of PDA size on the pulmonary vascular system.

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Objectives: To mitigate the shortage of homograft sources, the use of handmade trileaflet expanded polytetrafluoroethylene valves in pulmonary valve replacement has shown excellent results from multicentre studies conducted in Japan. However, world-wide data outside Japan are relatively insufficient. This study presents the long-term results of a single surgeon's use of flipped-back trileaflet method in a 10-year case series.

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Objectives: An extended newborn critical congenital heart disease (CCHD) screening program using oximetry has been implemented in Taipei, Taiwan since April 2014. This study was conducted to investigate the test accuracy and efficiency of this screening protocol.

Methods: This study analyzed data from 30 birthing facilities representing 87.

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Objective: To assess the effectiveness and safety of acupuncture for post-stroke fatigue (PSF).

Methods: Eight online databases were searched to collect relevant trials of acupuncture for PSF published before April 2021. Meta-analysis was performed by using RevMan 5.

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Background: Prenatal diagnosis of congenital heart disease (CHD) often leads affected families to experience psychological stress. Pediatric cardiology consultation is important in providing parents with sufficient information and reducing their anxiety to make an informed pregnancy decision. Involving a fetal nurse coordinator may optimize fetal anomaly care.

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Sudden infant death syndrome (SIDS), the most common cause of infant death in developed countries, is attributed to diverse trigger factors. Malignant cardiac dysrhythmias are potentially treatable etiologies, and congenital long QT syndrome (LQTS) is the most common cardiac ionic channelopathy confronted. β-Blockers or class Ib agents are the drugs of choice for the control of arrhythmias, and an implantable cardioverter defibrillator (ICD) should be considered for secondary prevention in survivors of lethal cardiac death.

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Major depressive disorder (MDD) is the second leading cause of disability worldwide. Currently, the structural magnetic resonance imaging-based MDD diagnosis models mainly utilize local grayscale information or morphological characteristics in a single site with small samples. Emerging evidence has demonstrated that different brain structures in different circuits have distinct developmental timing, but mature coordinately within the same functional circuit.

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Williams syndrome (WS) is a rare genetic disorder caused by the microdeletion of chromosome 7q11.23. Cardiovascular defects (CVDs) are the leading causes of morbidity and mortality in patients with WS.

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Background: Survivors of preterm birth are at risk of long-term cardiovascular consequences. The objective of this prospective observational study was to assess left heart function at preschool age in preterm children with very low birth weight (VLBW).

Methods: We recruited children aged 5-6 years from preterm infants and full-term children.

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Background: Prolongation of the QT interval is associated with the risk of sudden infant death syndrome. QT interval differs depending on age at the time of screening. Screening protocols have yet to be established for Taiwanese patients.

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Article Synopsis
  • The study included 106 ICR mice, divided into three groups: sham (normal), model (hypoxia-ischemia), and moxibustion-treated.
  • Results showed moxibustion improved behavioral performance and reduced brain damage compared to the model group, alongside increased SOD2 protein expression and decreased MDA levels, indicating potential protective effects.
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Article Synopsis
  • The study investigates the impact of moxibustion treatment on learning and memory in neonatal mice with hypoxic-ischemic encephalopathy (HIE), focusing on the expression of proteins associated with neural function.
  • It involved creating a HIE model in mice and then applying moxibustion therapy, observing brain tissue changes, protein expressions, and memory performance through tests like the Morris maze.
  • Results indicated that moxibustion reduced brain injury, increased important neuronal proteins (pCaMKⅡα and NeuN), and improved learning and memory capabilities compared to the untreated HIE model group.
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Coronavirus disease-19 (COVID-19) in children is usually mild but some are susceptible to a Kawasaki disease (KD)-like multisystem inflammatory syndrome in children (MIS-C) in the convalescent stage, posing a need to differentiate the phenotype, susceptibility, autoimmunity, and immunotherapy between KD and MIS-C, particularly in the upcoming mass vaccination of COVID-19. Patients with MIS-C are prone to gastrointestinal symptoms, coagulopathy, and shock in addition to atypical KD syndrome with fever, mucocutaneous lesions, lymphadenopathy, and/or cardiovascular events. MIS-C manifests KD-like symptoms that alert physicians to early recognize and adopt the KD treatment regimen for patients with MIS-C.

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Objective: The aim of this systematic review was to summarize and evaluate the existing evidence on the effectiveness and safety of acupuncture in relieving chronic pain-related depression (CPRD).

Methods: We searched seven online databases to identify eligible randomized controlled trials (RCTs) of acupuncture for CPRD published before September 2020. We included studies that used acupuncture as the intervention group, with or without a control group, and the control group was treated with conventional drugs.

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Article Synopsis
  • A study found that Taiwanese patients with mucopolysaccharidosis type II (MPS II) exhibit significant cardiac abnormalities, including high rates of valvular heart disease and cardiac hypertrophy, particularly as they age.
  • Echocardiograms analyzed showed notable deviations in various cardiac measurements, with the most common issue being mitral regurgitation, affecting over half of the patients.
  • Enzyme replacement therapy (ERT) resulted in improved left ventricular mass index over time compared to those not receiving treatment, but the overall severity of valvular issues continued to progress in both ERT and non-ERT groups.
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Autism spectrum disorder (ASD) is a range of neurodevelopmental disorders with behavioral and cognitive impairment and brings huge burdens to the patients' families and the society. To accurately identify patients with ASD from typical controls is important for early detection and early intervention. However, almost all the current existing classification methods for ASD based on structural MRI (sMRI) mainly utilize the independent local morphological features and do not consider the covariance patterns of these features between regions.

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Background: Cardiovascular abnormalities have been observed in patients with mucopolysaccharidosis (MPS) of any type, with the most documented abnormalities being valvular regurgitation and stenosis and cardiac hypertrophy. Only a few studies have focused on aortic root dilatation and the long-term effects of enzyme replacement therapy (ERT) in these patients.

Methods: We reviewed echocardiograms of 125 Taiwanese MPS patients (age range, 0.

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