Publications by authors named "Abdulmajeed AlSubaihin"
Article Synopsis
- The study explored the knowledge, attitudes, and intended practices of healthcare workers in Saudi Arabia towards the ChatGPT AI Chatbot shortly after its launch, using a survey of 1,057 participants.
- Findings indicated that while 18.4% had used ChatGPT for healthcare, a significant 84.1% of non-users were interested in using AI Chatbots in the future, with 75.1% feeling comfortable about its integration into healthcare practices.
- Despite recognizing the potential benefits in areas like medical research and decision-making, healthcare workers expressed concerns about the credibility of AI-generated information, highlighting the need for careful oversight before using AI Chatbots for diagnostic or treatment decisions.
With the increased discovery of genes implicated in vitamin D metabolism and the regulation of calcium and phosphate homeostasis, a growing number of genetic forms of rickets are now recognized. These are categorized into calciopenic and phosphopenic rickets. Calciopenic forms of hereditary rickets are caused by genetic mutations that alter the enzymatic activity in the vitamin D activation pathway or impair the vitamin D receptor action.
View Article and Find Full Text PDFBackground: Overweight and obesity have been observed in children with type 1 diabetes (T1D). This further increases their future risk of Cardiovascular Disease (CVD) as well as the development of other risk factors, such as dyslipidemia.
Aims: To compare lipid profiles in children and adolescents with Type 1 diabetes and lean mass (T1L), Type 1 diabetes and overweight or obese (T1OW/OB), and type 2 diabetes (T2D).
Unlabelled: We assessed the diagnostic utility of genetic panel testing to detect pathogenic variants associated with osteogenesis imperfecta in children presenting with multiple fractures. Thirty-five percent of children had a pathogenic variant. A history of a femur fracture or a first fracture occurring under 2 years of age were significant clinical predictors.
View Article and Find Full Text PDFBackground: Although Müllerian agenesis is the second most common cause of primary amenorrhea the underlying etiology in most cases is unknown. Müllerian agenesis has been reported as a rare finding associated with chromosomal aberrations of the 22q11 chromosomal region including at least 1 individual with cat eye syndrome (CES) and 10 individuals with deletions or duplications of the 22q11.2 region.
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