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http://dx.doi.org/10.1111/ans.18659 | DOI Listing |
Folia Morphol (Warsz)
December 2024
Department of Anatomical Dissection and Donation, Medical University of Lodz, Łódź, Poland.
The fibularis tertius (FT) is one of three muscles which constitute the anterior compartment of the leg. The anatomical variants of this muscle usually pertain to its origins, number of final tendons or points and shapes of insertions. In this case, it had an additional slip (AS) which originated from the same area as the main muscle belly and after descending along the extensor digitorum longus (EDL) it fused with one of its main tendons.
View Article and Find Full Text PDFAnat Sci Int
January 2025
Department of Anatomy, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Surg Radiol Anat
October 2024
Department of Neurosurgery, Tulane University School of Medicine, New Orleans, LA, USA.
J Funct Morphol Kinesiol
June 2024
Center for Anatomical Science and Education, Department of Surgery, Saint Louis University School of Medicine, Saint Louis, MO 63104, USA.
A novel combination of variations involving the extensor carpi radialis (ECR) muscle group was observed bilaterally in a 75-year-old female cadaver during routine dissection. An accessory tendon was observed arising from the extensor carpi radialis longus (ECRL) and traveling with the primary tendon through the second compartment of the extensor retinaculum. While the primary tendon inserted on the base of the second metacarpal, as is typical of ECRL, the accessory tendon inserted on the base of the third metacarpal.
View Article and Find Full Text PDFCongenit Anom (Kyoto)
November 2024
Department of Plastic Reconstructive and Aesthetic Surgery, Tekirdağ Namık Kemal University Faculty of Medicine, Tekirdağ, Turkey.
Polydactyly is typically observed as isolated and sporadic occurrences, although familial cases do exist, albeit with lower frequency, manifesting in various inheritance patterns. In around 30% of polydactyly cases, there exists a familial history, suggesting the probable involvement of a single gene. Given its potential for hereditary transmission, thorough investigation of the patients' parents, first-degree relatives, grandparents, and even great-grandparents for similar disorders becomes imperative.
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