Background: Allergic rhinitis (AR) is a disease that has significant effects on the quality of life of people and exhibits different phenotypic features with different clinical findings. By analyzing the data of pediatric patients, we aimed to reveal the relationship between demographic and laboratory data and clinical features and to gain awareness about allergic rhinitis phenotypes in children.
Methods: Demographic data, clinical complaints, physical examination findings, and atopy biomarkers are retrospectively analyzed to assess the impact of aeroallergens on the disease phenotype.
Results: In a study of 301 AR patients (median age 11 years; 66.1% male), sneezing (79.1%) was the most common complaint, and pallor of the nasal mucosa was the primary examination finding (83.1%). Persistent symptoms were reported by 62.1%, and 60.5% were polysensitized. Notably, 42.5% had asthma, often associated with concurrent sensitization to mold or animal dander (p ≤ 0.05). Pollen was the most prevalent allergen (65.8%), with significant increases in sensitization to pollen (p < 0.001) and animal dander (p = 0.003) with age. Patients with pollen sensitization reported more sneezing (p = 0.026) and persistent symptoms (p ≤ 0.05). Nasal congestion was predominantly seen in house dust mite-sensitized patients (78.4% with concha hypertrophy, p < 0.001). Overall, it was found that 59.7% of monosensitized patients and 63.7% of polysensitized patients reported persistent complaints.
Conclusion: This study, conducted in Western Turkey with 301 allergic rhinitis patients, revealed a high prevalence of polysensitization, particularly to pollen and animal dander. Polysensitized patients were older, exhibited higher IgE levels, and more frequently reported sneezing and rhinorrhea. Furthermore, polysensitization was linked to more persistent and severe symptoms, emphasizing the need for personalized treatment strategies for these patients. Our findings highlight the importance of developing individualized and region-specific approaches to enhance the effectiveness of allergic rhinitis management.
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http://dx.doi.org/10.1186/s12887-025-05541-8 | DOI Listing |
J Neural Eng
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Center for Neurorestoration and Neurotechnology, Providence VA Medical Center, Providence, RI, United States of America.
Advances in electronics and materials science have led to the development of sophisticated components for clinical and research neurotechnology systems. However, instrumentation to easily evaluate how these components function in a complete system does not yet exist. In this work, we set out to design and validate a software-defined mixed-signal routing fabric, 'xDev', that enables neurotechnology system designers to rapidly iterate, evaluate, and deploy advanced multi-component systems.
View Article and Find Full Text PDFAnn Med
December 2025
Department of Neonatology, Children's Hospital of Soochow University, Suzhou, China.
Aim: This review aims to summarize the epidemiology, pathogenesis, clinical features, management, prognosis and regression of Neonatal lupus erythematosus (NLE) with a view to providing directions for standardized diagnosis, treatment and further research.
Methods: We conducted a comprehensive literature review of NLE. NLE-related peer-reviewed papers were searched through PubMed/Medline were searched up to November 2024.
Background: T-lymphoblastic leukemia (T-ALL) is an aggressive hematologic malignancy with a less favorable prognosis. The genetic background of T-ALL is widely heterogeneous, with the co-occurrence of multiple genetic abnormalities. The STIL-TAL1 rearrangement results from a submicroscopic deletion on chromosome 1p33 and is present in 15 - 25% of T-ALL cases.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
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Trustwell Hospital, Banglore, India.
Lipomas are benign tumours composed of adipose tissue which are rare in paediatric age group, all the more infrequent over head and neck region. We report a case of 15 month old male child who presented with a history of swelling over the left side of the face for the duration and months. Patient was initially operated at 5 months of age elsewhere and presented to us with recurrence of the swelling at 15 months of age.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
January 2025
JIIU's Indian Institute of Medical Science and Research, Warudi, Badnapur, Maharashtra India.
In this case we report rare clinical entity of Millers syndrome in a small child of 6 years. It is basically an autosomal recessive condition characterized by anomalies of face and limbs such as malar hypoplasia, micrognathia, cleft lip and palate, restricted airway, bones and joints malformations [1, 2]. In this child apart from all these features we came across bleeding nasal masses attached to the inferior tubinates, which were causing complete nasal obstruction.
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