428 results match your criteria: "Mohammed VI University of Health Sciences.[Affiliation]"

Hamman syndrome, or spontaneous pneumomediastinum, is a rare condition characterized by the presence of free air in the mediastinum, often triggered by increased intrathoracic pressure from vomiting, coughing, or intense physical exertion. Its association with diabetic ketoacidosis (DKA) is extremely uncommon. We report a case of an 18-year-old male with poorly controlled type 1 diabetes who developed DKA complicated by pneumomediastinum, subcutaneous emphysema, and a small pneumothorax.

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Benign Acute Myositis in Children: A Case Series.

Cureus

November 2024

Paediatrics, Cheikh Khalifa International University Hospital, Mohammed V University, Faculty of Medicine and Pharmacy of Rabat, Casablanca, MAR.

Benign acute myositis is a rare and transient condition that usually occurs after a viral upper respiratory infection. Several viruses have been associated with this process particularly influenza B. Viral myositis frequently occurs in school-age children with a male predominance.

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Hepatic peliosis in a newborn - A case report and review of the literature.

Int J Surg Case Rep

December 2024

Department of Neonatal Resuscitation Unit, Cheikh Khalifa International University Hospital, Mohammed VI University of Sciences and. Health (UM6SS), Casablanca, Morocco; Department of Neonatal Resuscitation Unit, Mohammed VI International University Hospital, Mohammed VI University of Sciences and Health, Casablanca, Morocco.

Article Synopsis
  • Hepatic peliosis is a rare condition in which blood-filled spaces develop in the liver, often going unnoticed until autopsy; a case of a newborn with abdominal distension led to its discovery.
  • The newborn, just one day old, was found to have hepatomegaly and multiple blood cavities in the liver, confirmed through imaging and biopsy.
  • The only potential risk factor identified was the mother's use of antihistaminic drugs during pregnancy, suggesting a possible but unexplained link to this uncommon condition in neonates.
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Pediatric double-seropositive anti-glomerular basement membrane antibody disease: A case report and literature review.

Clin Nephrol Case Stud

November 2024

Department of Pediatrics, Cheikh Khalifa International University Hospital, Faculty of Medicine, Mohammed VI University of Health Sciences (UM6SS), Casablanca, Morocco.

Introduction: Glomerular basement membrane (GBM) disease is a severe and exceedingly rare disorder characterized by the presence of circulating antibodies targeting the non-collagen NC1 domain of the α3 chain of collagen type IV in glomerular and alveolar basement membranes. It typically presents as rapidly progressive glomerulonephritis (RPGN), often accompanied by pulmonary hemorrhage. The occurrence of double-seropositivity for anti-GBM antibody and anti-neutrophil cytoplasmic antibody (ANCA), primarily with myeloperoxidase specificity (MPO-ANCA), is particularly uncommon in pediatric cases.

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Background: Cogan syndrome is a rare autoimmune systemic vasculitis presenting with interstitial keratitis and audiovestibular symptoms. The atypical form, characterized by more extensive ocular lesions with audiovestibular symptoms appearing with a longer delay and more frequent systemic features, is usually underdiagnosed, delaying treatment.

Case Presentation: We report the case of a 30-year-old Mediterranean female who presented recurrent left red and painful eye.

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Introduction: Lung cancer management in patients with pacemakers presents unique challenges. This report examines the utilization of stereotactic body radiation therapy (SBRT) in such a patient population.

Case Presentation: A 75-year-old former smoker with a dual-chamber pacemaker presented with inoperable lung adenocarcinoma.

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Foreign body (FB) inhalation in children is a common and potentially life-threatening occurrence encountered in pediatric emergency medicine. A wide range of clinical presentations including often delayed onset of symptoms make it challenging to identify and provide a timely diagnosis. This increases the risk of complications and leads to suboptimal outcomes.

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Patient Safety in Anesthesiology: Progress, Challenges, and Prospects.

Cureus

September 2024

Epidemiology and Public Health, Laboratory of Community Health, Preventive Medicine and Hygiene, Faculty of Medicine and Pharmacy, Mohammed V University, Rabat, MAR.

Article Synopsis
  • - Anesthesiology has evolved significantly through advancements in technology and pharmacology, enhancing patient outcomes and enabling complex surgeries, but it still faces challenges and risks for both patients and healthcare professionals.
  • - The specialty is particularly challenged in low and middle-income countries, where collaborative actions and initiatives are essential to improve safety and access to anesthesia.
  • - Emerging technologies like simulation, genomics, artificial intelligence, and robotics offer potential solutions for enhancing patient safety in anesthesiology, but require careful ethical oversight and reliable research to maximize their benefits.
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Unstable Spinal Fracture With Arteria Lusoria: Management to Mitigate Aortic Risks.

Cureus

September 2024

Anesthesiology and Critical Care, Faculty of Medicine and Pharmacy, Hassan II University, Casablanca, MAR.

Article Synopsis
  • Aortic injuries related to unstable spinal fractures, although rare, can be life-threatening and require quick, collaborative medical responses to avoid serious complications.
  • A case study of a woman with a spinal fracture after a road accident highlighted the potential dangers of surgery without an aortic prosthesis, which could lead to severe bleeding, while using a prosthesis carries risks of mini-strokes and other complications.
  • The treatment approach involved using a thoracic prosthesis prior to spinal surgery, emphasizing the need for careful planning and consideration of the patient's unique anatomy to minimize risks of aortic injury during the surgical process.
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During the 3 years following the emergence of the COVID-19 pandemic, the African continent, like other regions of the world, was substantially impacted by COVID-19. In Morocco, the COVID-19 pandemic has been marked by the emergence and spread of several SARS-CoV-2 variants, leading to a substantial increase in the incidence of infections and deaths. Nevertheless, the comprehensive understanding of the genetic diversity, evolution, and epidemiology of several viral lineages remained limited in Morocco.

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Computational Drug Design Strategies for Fighting the COVID-19 Pandemic.

Adv Exp Med Biol

September 2024

Medical Biotechnology Laboratory (MedBiotech), Faculty of Medicine and Pharmacy, Bioinova Research Center, Mohammed Vth University, Rabat, Morocco.

The advent of COVID-19 has brought the use of computer tools to the fore in health research. In recent years, computational methods have proven to be highly effective in a variety of areas, including genomic surveillance, host range prediction, drug target identification, and vaccine development. They were also instrumental in identifying new antiviral compounds and repurposing existing therapeutics to treat COVID-19.

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The standard of care for locally advanced non-small-cell lung cancer (NSCLC) is either surgery combined with chemotherapy pre- or postoperatively or concurrent chemotherapy and radiotherapy. However, older and frail patients may not be candidates for surgery and chemotherapy due to the high mortality risk and are frequently referred to radiotherapy alone, which is better tolerated but carries a high risk of disease recurrence. Recently, immunotherapy with immune checkpoint inhibitors (ICIs) may induce a high response rate among cancer patients with positive programmed death ligand 1 (PD-L1) expression.

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Background: Hamstring injuries are a major problem in sports involving sprinting, such as soccer, rugby, and track and field, and lead to sports stoppages and psychological, social, and financial repercussions. For several years now, these injuries have been stagnating or even increasing. Preventing these injuries is therefore a fundamental issue for at-risk athletes.

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Locked posterior shoulder dislocations are dislocations that remain unreduced for more than three weeks. In most cases, they are associated with other injuries. We report the case of a 38-year-old male who presented with pain and total functional impotence due to a complex injury, including posterior glenohumeral dislocation, a reverse Hill-Sachs lesion, and a clavicle fracture.

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Article Synopsis
  • Mutations in the Spleen tyrosine kinase (Syk) protein greatly affect its function and treatment response, particularly in conditions like autosomal dominant hyper-IgE syndrome (AD-HIES).
  • The research involved analyzing 94 deleterious mutations in the Syk protein and screening a library of 997 compounds to find effective inhibitors tailored to these mutations.
  • Three promising inhibitors were identified through virtual screening, with ligand 1 (ID: 118558000) demonstrating the best stability and interactions, suggesting potential for improved therapies against Syk-related disorders.
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Basosquamous Carcinoma: A Rare Entity With an Atypical Presentation.

Cureus

August 2024

Dermatology Unit, Cheikh Khalifa International University Hospital, Mohammed VI University of Health Sciences, Casablanca, MAR.

Basosquamous carcinoma (BSC) is a rare entity of basal cell carcinomas. It is described as being nosologically at the border between a squamous cell carcinoma and a basal cell carcinoma, thus sharing characteristics of both entities. The frequency of this pathology remains low with a few cases reported in the literature.

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Identification of small molecule glucokinase activators for the treatment of diabetes based on plants from the traditional Chinese medicine: In silico analysis.

Microb Pathog

October 2024

Laboratory Biochemistry Environment and Agri-food, Department of Biology, Faculty of Science and Technics Mohammedia, Hassan II University Casablanca, Morocco. Electronic address:

Mutations in glucokinase (GCK) can either enhance or inhibit insulin secretion, leading to different forms of diabetes, including gestational diabetes. While many glucokinase activators (GKAs) have been explored as treatments, their long-term effectiveness has often been unsatisfactory. However, recent interest has surged with the introduction of dorzagliatin and TTP399.

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Phosphoinositide-3-kinases (PI3 K) are pivotal regulators of cell signaling implicated in various cancers. Particularly, mutations in the PIK3CA gene encoding the p110α catalytic subunit drive oncogenic signaling, making it an attractive therapeutic target. Our study conducted in silico exploration of 31 PIK3CA mutations across breast, endometrial, colon, and ovarian cancers, assessing their impacts on response to PI3Kα inhibitors and identifying potential non-toxic inhibitors and also elucidating their effects on protein stability and flexibility.

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Article Synopsis
  • - Desmoid tumors, although usually benign, can be aggressive, particularly when found in the anterior abdominal wall, as highlighted in a case involving a large 25 cm tumor in a 55-year-old obese patient with lymphedema.
  • - The patient underwent surgical removal of the tumor with a significant margin, including part of a muscle, and reconstruction using synthetic mesh, leading to improved lymphedema and limb function post-surgery.
  • - The case emphasizes the necessity for radical resection and proper reconstruction to improve long-term patient outcomes and suggests areas for further research on desmoid tumors.
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Lichen planopilaris (LPP) and its variants, mainly frontal fibrosing alopecia (FFA), affect the hair follicles, causing cicatricial alopecia. The condition has a significant negative impact on self-confidence and quality of life (QoL). This systematic review investigates the psychoemotional impact of LPP and its variants using the PRISMA guidelines.

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Article Synopsis
  • Rheumatologists have limited knowledge about patients' use of complementary and alternative medicine (CAM) for rheumatic diseases, making it important to understand its prevalence and benefits to enhance patient care.
  • A study conducted at a Moroccan University Hospital found that 46% of participants used at least one CAM method, with cupping therapy being the most popular (36%), primarily for pain relief (55%).
  • The study indicated that patients with higher education levels were significantly less likely to use CAM, highlighting the influence of education on treatment choices and the perceived effectiveness of different CAM approaches.
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Article Synopsis
  • Primary malignant bone tumors and metastases can arise in the proximal femur, requiring surgical treatment for either palliative or curative purposes.
  • Curative treatment involves two main stages: removing the tumor through wide excision with sufficient margins and reconstructing the affected bone and soft tissue to restore function.
  • Reconstruction methods vary, including composite or massive prostheses and options for joint reconstruction like hemiarthroplasty, intermediate prosthetics, or total hip replacement.
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Article Synopsis
  • Syndromic hearing loss (SHL) is a condition involving hearing impairment and other health issues, with over 400 known syndromes, making early diagnosis crucial for managing associated risks.
  • This study analyzed the genetic causes of hearing loss in three Moroccan patients using whole exome sequencing, discovering specific mutations linked to Perrault syndrome and D-bifunctional protein deficiency.
  • The findings emphasize the power of whole exome sequencing and bioinformatics in identifying harmful genetic mutations and understanding their impacts on protein function.
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Human Genetic and Immunological Determinants of SARS-CoV-2 Infection and Multisystem Inflammatory Syndrome in Children.

Clin Exp Immunol

July 2024

Laboratory of Clinical Immunology, Inflammation and Allergies (LICIA), Faculty of Medicine and Pharmacy, Hassan II University, Casablanca 20250, Morocco.

Article Synopsis
  • SARS-CoV-2 causes pneumonia and severe respiratory issues, especially in patients with genetic defects in type I interferon, impacting individuals differently based on age and gender.
  • About 3-5% of critical COVID-19 patients under 60 years have genetic defects in interferon production, while around 15-20% of those over 70 show autoantibodies against type I interferons.
  • This review discusses the links between genetic and immunological factors contributing to severe COVID-19 and pediatric multisystem inflammatory syndrome (MIS-C), emphasizing the need for more research to develop targeted treatments and strategies for future viral infections.
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