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J Ayub Med Coll Abbottabad
December 2024
Department of Pulmonology.
Thromb Res
December 2024
Division of Cardiology, Department of Medicine, NYU Grossman School of Medicine, New York, NY, USA.
Background And Aims: Patients with intermediate-risk pulmonary embolism (PE) commonly present with a significantly reduced cardiac index (CI). However, the identification of this more severe profile requires invasive hemodynamic monitoring. Whether inferior vena cava (IVC) contrast reflux, as a marker of worse right ventricular function, can predict invasive hemodynamics has not been explored.
View Article and Find Full Text PDFCureus
August 2024
Department Otorhinolaryngology-Head and Neck Surgery, Hospital Universiti Sains Malaysia, Universiti Sains Malaysia, Kelantan, MYS.
Isolated sphenoid sinusitis (ISS) is a rare but potentially serious condition, often leading to severe complications due to delayed diagnosis and treatment. This case report discusses a 75-year-old male with type 2 diabetes mellitus who presented with severe left-sided headache and neck pain. Diagnostic imaging revealed isolated sphenoid sinusitis with prevertebral extension, a rare occurrence that highlights the potential for deep neck space involvement.
View Article and Find Full Text PDFPan Afr Med J
September 2024
Department of Pediatrics and Child Health, Aga Khan University Hospital, Nairobi (AKUHN), Nairobi, Kenya.
Introduction: COVID-19 infection has attracted global attention with limited published data on the burden in African children.
Methods: hospital-based longitudinal survey in children with COVID-19 infection, aged 0-18 years admitted between August 2020 and December 2021. The main objective of the study was to describe socio-demographic, clinical and diagnostic manifestations of COVID-19 infection in children.
Eur J Hum Genet
December 2024
UCL Institute of Ophthalmology, University College London, London, UK.
Corneal dystrophies are phenotypically and genetically heterogeneous, often resulting in visual impairment caused by corneal opacification. We investigated the genetic cause of an autosomal dominant corneal stromal dystrophy in a pedigree with eight affected individuals in three generations. Affected individuals had diffuse central stromal opacity, with reduced visual acuity in older family members.
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