Archived Articles
Case Report | Open Access
Published on: 31 Jan 2026
Article ID: wjo.2026.a3102
Familial Metachronous Wilms’ Tumour in a Sibling with Previous Bilateral Synchronous Wilms’ Tumour: A Rare Familial Cluster
Wilms Tumour (WT) is the most common renal malignancy of childhood, typically occurring sporadically. Familial WT accounts for fewer than 2% of cases and often involves germline predisposition syndromes. Metachronous WT in siblings - particularly when one sibling previously presented with bilateral synchronous disease - is exceptionally rare. We report a case of a child presenting with unilateral WT whose older sibling had been treated several years earlier for bilateral synchronous WT. This…
Research Article | Open Access
Published on: 24 Sep 2025
Article ID: wjo.2025.i2401
The Effect of Egyptian Women’s Breast Milk on the Breakdown of Liver Tumor Cells
Breast milk is a complex biological fluid rich in immunological and bioactive components, traditionally studied for its benefits in infant immunity. Recent evidence suggests that breast milk may also possess anticancer properties. This study introduces a novel hypothesis: Egyptian women's breast milk, potentially influenced by unique dietary and environmental factors, may contain bioactive compounds capable of targeting liver tumor cells. We present the scientific rationale for this…
Research Article | Open Access
Published on: 24 Sep 2025
Article ID: wjo.2025.i2402
The Use of Breast Milk in Treating Adult Diseases: Myth or Medicine
Breast milk, long recognized as the optimum beginning of nutrition and invulnerable guardianship for babies, has recently attracted interest in its potential healing applications for adult diseases. This arising district of research, though still in its babyhood, desires that bioactive elements in bosom milk—such as lactoferrin, lysozyme, immunoglobulin A (IgA), and the malignancy-point in a direction complex HAMLET (Human Alpha-lactalbumin Made Lethal to Tumor containers)—can play a…
Research Article | Open Access
Published on: 24 Sep 2025
Article ID: wjo.2025.i2407
Gene Therapy in the Treatment of Inherited Genetic Disorders: Current Developments and Challenges
Gene therapy has emerged as a groundbreaking approach to address inherited genetic disorders, offering the potential to target and correct genetic mutations at the cellular level. This innovative technique involves altering the genetic material within a patient’s cells to correct mutations responsible for diseases such as cystic fibrosis, muscular dystrophy, and hemophilia. Advancements in technologies like CRISPR-Cas9 have significantly improved the accuracy and efficiency of DNA editing,…
DOI: 10.5281/zenodo.18497845 »