756 results match your criteria: "Hôpital universitaire des enfants Reine Fabiola[Affiliation]"

: Hydrolysed rice formula (HRF) is tolerated by >90% of children with cow's milk protein allergy (CMPA). However, concerns have been raised about potential suboptimal growth in infants fed HRF compared to those fed an extensively hydrolysed milk protein formula (eHF). : To compare growth, safety and tolerance acquisition in infants with CMPA when fed HRF versus eHF.

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Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series.

Hum Reprod Open

December 2023

Department of Internal Medicine and Pediatrics, Ghent University, Pediatric Endocrinology Service, Ghent University Hospital, Belgium, Ghent.

Article Synopsis
  • - The study investigates the long-term effects of bilateral testicular regression (BTR) in individuals, focusing on growth and development outcomes, particularly highlighting suboptimal penile growth often related to genetic factors.
  • - BTR, a rare condition with potential vascular and genetic origins, was analyzed in a cross-sectional study involving 35 participants recruited from eight pediatric endocrinology departments in Belgium over three years.
  • - Key findings revealed common maternal complications during pregnancy and identified specific genetic variants in some participants, while a centralized review of gonadal tissue contributed to understanding the condition's clinical implications.
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Objectives: The Phase 3 Study 338 (NCT02834793) assessed long-term clinical outcomes of adjunctive perampanel in patients ≥2 years of age with uncontrolled seizures associated with Lennox-Gastaut syndrome (LGS).

Methods: Eligible patients were diagnosed with LGS and receiving one to four concomitant antiseizure medications with an average of two or more drop seizures/week during baseline. The study comprised an 18-week double-blind, randomized, placebo-controlled Core Study and ≥52-week open-label Extension.

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Unlabelled: Newborn screening for cystic fibrosis (CF-NBS) using an IRT-DNA algorithm with a 12 CFTR-variant panel and an IRT/IRT failsafe was officially implemented in the French-speaking Community of Belgium in January 2020. This screening protocol was evaluated after 4 years according to the criteria defined by the European Cystic Fibrosis Society's working group on neonatal screening. Immunoreactive trypsinogen concentration (IRT) was measured on dried blood spots collected between the second and the fourth day of life.

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Background: Previous findings demonstrated that healthcare workers with a high level of social support are likely to engage in their work. Healthcare workers are not only engaged in the physical problems of their patients but also in their emotional difficulties. Pediatric professionals must express and regulate their own emotions during their interactions with young patients and their families.

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Article Synopsis
  • * In a study using a mouse model of DMD (mdx mice), researchers found that the absence of dystrophin led to altered firing of Purkinje cells and unusual brain oscillations, but these changes weren’t caused by problems with calcium-binding proteins.
  • * The mdx mice also showed signs of cerebellar dysfunction, including severe muscle weakness and coordination issues, suggesting a possible link between cerebellar impairments and cognitive deficits seen in humans with DMD. *
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Rare Oncogenic Fusions in Pediatric Central Nervous System Tumors: A Case Series and Literature Review.

Cancers (Basel)

September 2024

Department of Pathology, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Erasme University Hospital, 1070 Brussels, Belgium.

Central Nervous System (CNS) pediatric tumors represent the most common solid tumors in children with a wide variability in terms of survival and therapeutic response. By contrast to their adult counterpart, the mutational landscape of pediatric CNS tumors is characterized by oncogenic fusions rather than multiple mutated genes. CNS pediatric tumors associated with oncogenic fusions represent a complex landscape of tumors with wide radiological, morphological and clinical heterogeneity.

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Paradoxical metabolic acidosis after vomiting in children with spinal muscular atrophy: A report of 9 patients.

Arch Pediatr

October 2024

Pediatric Neurology & Intensive Care Unit, Assistance Publique des Hôpitaux de Paris, Hôpital Raymond-Poincaré, Garches, France; Simone Veil Health Science Center, Université Versailles SQY, Paris-Saclay, France.

Article Synopsis
  • Spinal muscular atrophy (SMA) leads to severe metabolic acidosis in patients after mild vomiting, a serious and uncommon condition that can result in life-threatening complications.
  • A study of 11 SMA patients revealed a median pH of 7.23 and low bicarbonate levels, with nearly half showing signs of ketoacidosis; hydration with glucose significantly improved their condition within 24-48 hours.
  • The findings suggest that SMA patients are more vulnerable to ketoacidosis from fasting and have impaired buffering capacity, highlighting the need for prompt treatment to prevent exhaustion and potentially fatal outcomes.
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What Is Known: Botulinum toxin (BoNT) causes muscle relaxation by inhibiting acetylcholine release from presynaptic motor neurons at the neuromuscular junction.

What Is New: In children with achalasia, BoNT can be considered only in patients in whom rapid weight gain is important to improve surgical outcomes. BoNT has been suggested for treating cricopharyngeal achalasia and delayed gastric emptying.

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Article Synopsis
  • - The study analyzed treatment decisions for H. pylori infection in children using data from the EuroPedHp Registry, focusing on various factors influencing whether or not therapy was administered, especially regarding gastrointestinal (GI) comorbidities.
  • - Out of 1165 pediatric patients, those with GI comorbidities were significantly less likely to receive eradication treatment (only 57%) compared to those with no comorbidities (89%) despite having similar symptoms and conditions.
  • - The findings suggest that H. pylori-infected children with GI issues had a much lower chance (75% reduced) of receiving treatment, indicating no rationale for different management approaches based on GI comorbidities in pediatric patients with confirmed infections.
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Imaging features of posterior microphthalmos.

J Fr Ophtalmol

November 2024

Service d'ophtalmologie, Erasme Hospital, hôpital universitaire de Bruxelles (HUB), université Libre de Bruxelles (ULB), Bruxelles, Belgium; Service d'ophtalmologie, hôpital universitaire de Bruxelles (HUB), hôpital universitaire des enfants Reine-Fabiola (HUDERF), université libre de Bruxelles (ULB), Bruxelles, Belgium.

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Background: Factors associated with severe COVID-19 infection have been identified; however, the impact of infection on longer-term outcomes is unclear. The objective of this study was to examine the impact of COVID-19 infection on the trajectory of lung function and nutritional status in people with cystic fibrosis (pwCF).

Methods: This is a retrospective global cohort study of pwCF who had confirmed COVID-19 infection diagnosed between January 1, 2020 and December 31, 2021.

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The enduring impact of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its disease manifestation, COVID-19, on public health remains significant. Postacute sequelae of SARS-CoV-2 infection (PASC) affect a considerable number of patients, impairing their quality of life. While the role of the cytokine storm in acute COVID-19 is well established, its contribution to the pathophysiology of PASC is not fully understood.

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Objective: To assess and compare the value of antenatally determined observed-to-expected (O/E) lung-area-to-head-circumference ratio (LHR) on ultrasound examination vs O/E total fetal lung volume (TFLV) on magnetic resonance imaging (MRI) examination to predict postnatal survival of fetuses with isolated, expectantly managed left-sided congenital diaphragmatic hernia (CDH).

Methods: This was a multicenter retrospective study including all consecutive fetuses with isolated CDH that were managed expectantly in Mannheim, Germany, and in five other European centers, that underwent at least one ultrasound examination for measurement of O/E-LHR and one MRI scan for measurement of O/E-TFLV during pregnancy. All MRI data were centralized, and lung volumes were measured by two experienced operators blinded to the pre- and postnatal data.

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Hypothyroidism due to biallelic variants in IYD: description of 4 families and a novel variant.

Eur J Endocrinol

August 2024

Paediatric Endocrinology Unit, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (H.U.B.), Hôpital Universitaire des Enfants Reine Fabiola (HUDERF), 1020 Bruxelles, Belgium.

Biallelic loss-of-function variants in the IYD gene cause hypothyroidism resulting from iodine wasting. We describe 8 patients (from 4 families in which the parents are first cousins) who are homozygous for a variant in IYD (including a novel missense deleterious variant, c.791C>T [P264L], in 1 family).

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Insight into the role of TXNRD2 in steroidogenesis through a novel homozygous TXNRD2 splice variant.

Eur J Endocrinol

August 2024

Division of Pediatric Endocrinology, Diabetology and Metabolism, Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Article Synopsis
  • This study is about how a specific gene (TXNRD2) impacts adrenal cortisol production, which is important for our body's stress response.
  • Researchers looked at a patient with a rare gene change that caused problems with cortisol production, leading to health issues.
  • They found that the gene mutation led to increased harmful substances in the body and reduced the ability to make cortisol, which is vital for health.
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Background: The authors report the prospective evaluation of reduced dose alkylator chemotherapy combined with radiotherapy for European Pediatric Soft Tissue Sarcoma Study Group (EpSSG) standard risk nonalveolar rhabdomyosarcoma (NA-RMS).

Patients And Methods: Localized node negative Intergroup Rhabdomyosarcoma Study (IRS) II/III NA-RMS at favorable sites (subgroup C), <25 years old, received five cycles of ifosfamide, vincristine, and dactinomycin (IVA) chemotherapy (30 g/m ifosfamide) and four cycles of vincristine and dactinomycin (if receiving radiotherapy), or nine cycles of IVA (54 g/m ifosfamide) ± radiotherapy. Delayed primary tumor excision was considered for IRS III tumors.

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Cognition and communication in patients with spinal muscular atrophy: A systematic review.

Heliyon

July 2024

Université Libre de Bruxelles, ULB, Hôpital Universitaire de Bruxelles (HUB), Hôpital Universitaire des Enfants Reine Fabiola (HUDERF), Department of Paediatric Neurology and Neuromuscular Reference Center, Brussels, Belgium.

•Synthesizes evidence from 12 studies on cognitive and communicative impacts in SMA, focusing on nuanced functional outcomes.•Highlights cognitive variability in SMA1, revealing subtle challenges in SMA2 and 3, and stresses tailored assessment methodologies.•Identifies communication barriers in SMA, emphasizing the urgency of investigating their potential interplay with cognitive functions.

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Childhood craniopharyngioma: a retrospective study of children followed in Hôpital Universitaire de Bruxelles.

Front Endocrinol (Lausanne)

July 2024

Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Department of Pediatrics, Brussels, Belgium.

Introduction: Craniopharyngiomas (CPs) are benign brain tumors accounting for 5 - 11% of intracranial tumors in children. These tumors often recur and can cause severe morbidity. Postoperative radiotherapy efficiently controls and prevents progression and recurrence.

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Unlabelled: Idiopathic focal unilateral skull thinning is a rare finding. An explanation, such as trauma or disease, can often be found. However, in some cases, no explanation is forthcoming, and thus, we must look further into their history for a possible cause.

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Article Synopsis
  • Many kids feel anxious and scared before medical procedures, especially when they have to get an MRI, which is a big machine that takes pictures of the inside of your body.
  • Researchers tested if using virtual reality (VR) could help reduce this anxiety by letting kids experience a pretend MRI with sounds and sights before their actual appointment.
  • The study found that kids who used VR felt less anxious before their MRI, which could help make the experience easier for them, even though it didn't change the success rate of the MRI itself.
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Background: Respiratory and bulbar dysfunctions (including swallowing, feeding, and speech functions) are key symptoms of spinal muscular atrophy (SMA), especially in its most severe forms. Demonstrating the long-term efficacy of disease-modifying therapies (DMTs) necessitates an understanding of SMA natural history.

Objective: This study summarizes published natural history data on respiratory, swallowing, feeding, and speech functions in patients with SMA not receiving DMTs.

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Article Synopsis
  • * A study involving 99 SMA type I-III patients examined the perceptions of treatment benefits among different outcome groups, consisting of those with significant, non-significant, or no improvement after 15 months of treatment.
  • * The findings indicate that there is little difference in how patients and caregivers perceive the benefits of treatment among the different groups, suggesting that standard functional scales may not fully capture their real-life experiences with the treatment.
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Protection of Telomeres Protein 1 (POT1) protein is an essential subunit of the shelterin telomere binding complex, regulating telomere length. Some POT1 gene pathogenic variants (PV) lead to telomere elongation, genomic instability and higher risk of cancer. POT1 tumour predisposition syndrome (POT1-TPD) has autosomal dominant inheritance and unknown penetrance.

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An increasing number of studies have highlighted the existence of a sex-specific immune response, wherein men experience a worse prognosis in cases of acute inflammatory diseases. Initially, this sex-dependent inflammatory response was attributed to the influence of sex hormones. However, a growing body of evidence has shifted the focus toward the influence of chromosomes rather than sex hormones in shaping these inflammatory sex disparities.

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