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http://dx.doi.org/10.23736/S2784-8671.21.07097-3 | DOI Listing |
Network
December 2024
School of Computing, Asia Pacific University of Technology & Innovation, Kuala Lumpur, Malaysia.
Skin melanin lesions are typically identified as tiny patches on the skin, which are impacted by melanocyte cell overgrowth. The number of people with skin cancer is increasing worldwide. Accurate and timely skin cancer identification is critical to reduce the mortality rates.
View Article and Find Full Text PDFRadiol Case Rep
January 2025
Department of Radiology National Institute of Oncology, University Mohammed V of Rabat, Rabat, Morocco.
Plexiform neurofibroma is characterized by diffuse intraneural neoplastic overgrowth involving a long nerve segment, with tortuous expansion of its branches. It is a hallmark of Neurofibromatosis Type 1 (NF1). We report the case of a 36-year-old man with a known diagnosis of NF1, who was admitted for chronic posterior cervical pain and cervicobrachial neuralgia.
View Article and Find Full Text PDFCureus
October 2024
Department of Surgery, University of South Florida Morsani College of Medicine, Tampa, USA.
Small bowel diverticulosis can occur anywhere in the small bowel but is most common in the duodenum. Jejunoileal diverticulosis is much less common and tends to have a more chronic, nonspecific disease course. In the literature, this condition has a higher incidence in men in their sixth and seventh decades of life.
View Article and Find Full Text PDFJ Ultrason
November 2024
Department of Anatomy, Jagiellonian University, Kraków, Poland.
Clin Case Rep
November 2024
Department of Human Genetics University Medicine Greifswald, and Interfaculty Institute of Genetics and Functional Genomics, University of Greifswald Greifswald Germany.
Key Clinical Message: Not only germline but also postzygotic mutations in the or genes can lead to capillary malformation-arteriovenous malformation (CM-AVM) syndrome. As it is not always possible to clinically distinguish between constitutional variants and postzygotic mosaicism, a sufficiently high sequencing depth must be used in genetic diagnostics to detect both.
Abstract: Capillary malformation-arteriovenous malformation (CM-AVM) syndrome, with or without Parkes Weber syndrome, is a rare autosomal dominant disease caused by pathogenic or variants.
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