Publications by authors named "Fallahpour M"

Background: Hymenoptera venom allergy is a potentially severe allergic reaction in the general population. The only preventative approach in these cases is venom immunotherapy (VIT), which follows different protocols. The recommended initial dose is 0.

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  • The study aimed to compare the efficacy, safety, and immunogenicity of a new treatment (P043) for allergic asthma with the established drug, Xolair (omalizumab), focusing on the rate of asthma exacerbations.
  • Over a 28-week trial with 256 participants, results showed that both treatments had similar rates of exacerbations, asthma control test scores, and spirometry measurements, indicating that P043 is as effective as omalizumab.
  • Adverse events reported were comparable between both groups, with common issues being dyspnea and headache, and no significant issues with drug safety or immunogenicity observed for either treatment.
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  • Common variable immunodeficiency (CVID) is a significant disorder characterized by both infectious and noninfectious complications, with 66.4% of patients experiencing noninfectious issues such as enteropathy and autoimmunity.
  • In a study of 387 CVID patients, those with B-cell lymphopenia showed higher rates of certain complications, particularly in the dermatologic, endocrine, and musculoskeletal systems.
  • The study highlights the need for routine monitoring and appropriate treatment strategies, including medication alongside immunoglobulin therapy, to manage complications associated with CVID effectively.
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  • - The study focused on 16 Iranian patients with very early-onset inflammatory bowel disease (VEO-IBD), aiming to explore the role of underlying genetic issues related to inborn errors of immunity (IEI) in this condition.
  • - Most patients were young (median age of 43.5 months), with symptoms starting around 4 months; common signs included chronic diarrhea and perianal diseases, with a notable prevalence of consanguinity among parents.
  • - Whole exome sequencing (WES) revealed genetic variants in 81.3% of patients, highlighting notable gene mutations like IL10RB, and emphasizing the need for genetic evaluation in early-onset IBD cases due to the high incidence of mon
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Background: The poly-sensitization to Hymenoptera venom makes it difficult to select genuine allergens for immunotherapy and increases patients' costs. The objective of this study was to determine the culprit allergen in dual or triple-sensitized patients to three Hymenoptera venoms through molecular diagnosis and evaluating the results of incorporating the molecular diagnosis with skin tests.

Methods: Thirty-two patients with anaphylactic reactions and dual or triple-sensitization to Hymenoptera venoms in skin tests entered this study.

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Background: Chronic Rhinosinusitis (CRS) is a paranasal sinus inflammatory disease and is divided into two subgroups defined as CRS with nasal polyps (CRSwNP) and CRS without nasal polyps (CRSsNP). CRSwNP displays a T helper (Th)2 biased phenotype, and based on sensitivity or tolerance to aspirin or non-steroidal anti-inflammatory drugs (NSAID), is further subdivided into Aspirin-exacerbated respiratory disease (AERD) and non-AERD groups. Considering the challenge of diagnosis and treatment in patients with CRSwNP, particularly the AERD subtype, and the significance of endotyping in these patients, we examined the immune profile and endotyping based on gene expression analysis in the AERD and the non-AERD groups of patients with CRSwNP.

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  • Severe combined immunodeficiencies (SCIDs) are genetic disorders leading to malfunctioning immune systems due to issues with T and B cells, with many cases linked to RAG mutations.
  • This report details two siblings who both had SCID caused by a new mutation in the RAG2 gene, affecting their immune responses and leading to serious health complications.
  • The findings emphasize the importance of ongoing research to better understand the mutation's effects, as well as improving communication among healthcare professionals to enhance patient care.
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This case report describes our experience of surgical strategies of two patients with neglected subaxial cervical spine fracture-dislocation that came to our center with subsequent follow-ups. Subaxial cervical spine fracture-dislocation must be immediately diagnosed and treated. However, it can be neglected in some cases, especially in developing health care systems and patients with low socioeconomic status.

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The cervical spinal canal has a wide range of motion and specific biomechanics involved with different pathologies that may cause dynamic cord compressions. This study has introduced new protocol for acquiring an extension view of cervical MRI to assess dynamic cervical spinal canal compromise. We posit that dynamic MRI comprising extension view in prone position could be a practical option when deciding the best approach in treating challenging patients.

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  • - Severe combined immunodeficiency (SCID) is a serious genetic disorder affecting the immune system, leading to critical infections, with variances in disease presentation complicating timely diagnosis.
  • - A study described four patients, including both typical and atypical SCID cases, who showed symptoms within six months of birth with various genetic mutations identified, such as in the RAG2, IL7R, ADA, JAK3, LIG4, and LAT genes.
  • - The findings provide insights into the genetic diversity of SCID and emphasize the importance of early diagnosis and management for affected individuals, including the confirmation of mutations through Sanger sequencing in both patients and their parents.
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  • NSAID-exacerbated respiratory disease (N-ERD) is a complex condition diagnosed mostly through aspirin challenge tests, which can be risky and time-consuming.
  • This study followed patients undergoing standard medical treatment for three months, measuring symptom severity using the Sinonasal Outcome Test (SNOT22).
  • Results indicated that aspirin sensitivity in patients was not reliably predicted by the severity of their symptoms or by their improvement after treatment, with both aspirin-sensitive and tolerant patients showing similar symptom reductions.
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Beta-lactam (BLM) antibiotics, including amino-penicillin and cephalosporins, are typically the first-choice treatment for bacterial infections. However, adverse reactions to these antibiotics are frequently reported, causing non-allergist physicians to select alternative broad-spectrum antibiotics that can have harmful consequences. Patients with unclear histories of hypersensitivity reactions to BLMs should undergo an allergy workup to establish a firm diagnosis, particularly when different drugs are prescribed simultaneously.

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Background: Clinical trials were conducted on children on side effects after vaccination. We tried to assess the frequency and onset of the main symptoms in children who were vaccinated. We aimed to evaluate early and delayed adverse effects after coronavirus disease 2019 (COVID-19) vaccine among Iranian pediatrics and adolescents in a national survey.

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Background: The two main pillars of asthma management include regular follow-up and using guidelines in the treatment process. Patient portals enable regular follow-up of disease, and guideline-based decision-support-systems can improve the use of guidelines in the treatment process. Based on the Global Initiative for Asthma (GINA) and Snell's drug interaction, asthma management system in primary care (AMSPC) includes the capabilities of both mentioned systems.

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Introduction: Echinococcosis is a chronic disease caused by Echinococcus species. The central nervous system (CNS) hydatidosis is still a major concern, especially in endemic countries, due to non-specific features and late diagnosis and treatment. This study aimed to provide a systematic review to elucidate the epidemiology and clinical characteristics of CNS hydatidosis worldwide over the past decades.

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Background: Chronic rhinosinusitis with nasal polyps (CRSwNP) is a complex disorder and effective treatment remains a major challenge. Some antibiotics with anti-inflammatory properties are reported to have potential to be used as an adjunct therapy in the management of chronic airway inflammation.

Objective: The aim of this study was to evaluate the efficacy of doxycycline in CRSwNP.

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Genetic defects in the development, maturation, and/or function of the immune cells can lead to Inborn errors of immunity (IEI) which may predispose patients to malignancies. The overall risk for cancer in children with IEI ranges from 4 to 25% and the type of malignancy is highly dependent on the specific mutant gene underlying IEI. We investigated 3056 IEI patients registered in the Iranian national registry between the years 1999 and 2020 in this retrospective cohort study.

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Coronavirus disease 2019 (COVID-19) affects millions of people worldwide. Clinical manifestations range from asymptomatic to severe viral pneumonia. CVID patients with COVID-19 infection are not adequately studied.

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  • - Type 2 Griscelli syndrome (Type 2 GS) is a genetic immune disorder characterized by hypopigmentation and varies in severity of neurological and immunodeficiency symptoms across its types, with specific genetic mutations identified for each type.
  • - Hemophagocytic lymphohistiocytosis (HLH) is a serious condition marked by severe inflammation, which can be either primary or secondary, often associated with autoimmune diseases, infections, or cancers.
  • - The text discusses a case of type 2 GS in a newborn who developed HLH due to a prenatal infection, highlighting the link between prenatal infections and severe complications like HLH.
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Background And Aims: Thalassemia syndromes are the most common hemoglobinopathy globally related to blood transfusion and iron overload in the body. Splenectomy, excessive iron overload, and repeated exposure to antigens in blood transfusions can cause severe damage to the patient's immune system making the patient prone to frequent infection. This study evaluates the immune system status and infection rate in beta-thalassemia major patients receiving iron chelators.

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Background: Research suggests that participation in activities has the potential to prevent or delay the development of later-life cognitive decline and dementia. This area is unexplored within occupational therapy.

Aim: To explore and describe the clinical reasoning of occupational therapists in selecting activities together with older adults with dementia to participate in, with the goal to postpone further development of cognitive decline in a sample from the German part of Switzerland.

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Introduction: Identifying strategies to prevent or delay cognitive decline among the rising numbers of elderly is acknowledged as a global public health priority. Research suggests that an active lifestyle in terms of participation in activities has the potential to reduce the risk of later-life cognitive decline. The concept of "active everyday life", however, needs to be further explored.

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Objective: Sesame allergy is the most prevalent allergy to seeds. Oral immunotherapy (OIT) is defined as continuous consumption of an allergen at special doses and time. Omalizumab (Anti-IgE) increases tolerance to allergens used in OIT.

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The purpose of this research was to investigate the gene expression levels of inflammatory cytokines interferon (IFN), tumor necrosis factor (TNF), interleukin (IL)1, IL2, IL6, IL8, and IL17, and anti-inflammatory cytokines IL4, IL10, IFN, and IFN, as well as relevant key transcription factors (TFs), including GATA3, PU1, NF-B (nuclear factor kappa-light-chain-enhancer of activated B cells), IRF3 (interferon regulatory factor 3), BCL6 (B cell lymphoma 6 protein), FOXP3 (forkhead box P3), RORt, and T-bet (T-box expressed in T cell) in Iranian patients with moderate and severe coronavirus disease 2019 (COVID-19). Fifty-six patients with COVID-19, and 25 healthy controls (HCs) age and sex matched were investigated. Based on the interim guidance of COVID-19 from the World Health Organization, the patients were classified into 33 moderate and 23 severe patients with COVID-19.

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