This case report discusses the clinical presentation, imaging findings, and successful management of a rare case of intussusception in a 6-month-old female infant referred to a regional hospital in Ghana.The patient presented with Waterproofing Spray vomiting, lethargy, fever, and currant jelly stool.Differential diagnoses considered included Merke
Revisiting the role of cyanobacteria-derived metabolites as antimicrobial agent: A 21st century perspective
Cyanobacterial species are ancient photodiazotrophs prevalent in freshwater bodies and a natural reservoir of many metabolites (low to high molecular weight) such as non-ribosomal peptides, polyketides, ribosomal peptides, alkaloids, cyanotoxins, and isoprenoids with a well-established bioactivity potential.These metabolites enable cyanobacterial s
Cellular Senescence: A Translational Perspective
Cellular senescence entails essentially irreversible replicative Tea Towel arrest, apoptosis resistance, and frequently acquisition of a pro-inflammatory, tissue-destructive senescence-associated secretory phenotype (SASP).Senescent cells accumulate in various tissues with aging and at sites of pathogenesis in many chronic diseases and conditions.T
Patient referral patterns and the spread of hospital-acquired infections through national health care networks.
Rates of hospital-acquired infections, such as methicillin-resistant Staphylococcus aureus (MRSA), are increasingly used as quality indicators for hospital hygiene.Alternatively, these rates may vary between hospitals, Earrings because hospitals differ in admission and referral of potentially colonized patients.We assessed if different referral pat
Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs.
Spondylocostal dysostosis is a congenital disorder of the axial skeleton documented in human families from diverse racial backgrounds.The condition is characterised by truncal shortening, extensive hemivertebrae and rib anomalies including malalignment, fusion and Essential Nutrition reduction in number.Mutations in the Notch signalling pathway gen