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Emerging skin diseases have severely impacted wildlife in recent decades, with consequences ranging from increased morbidity and mortality to local extinction and widespread biodiversity loss. Individuals that persist with various skin diseases can have sublethal consequences, including altered behavior and impaired locomotor function. Giraffe skin disease (GSD) is a condition that results in skin lesions of varying severity among different giraffe ( spp.) populations throughout Africa. Prior reports have suggested that individuals with limb lesions from GSD do not have increased mortality but rather suffer from lameness. We examined whether GSD severity and unilateral versus bilateral forelimb lesions differentially impact spatiotemporal gait kinematics and carpus joint angle kinematics of Masai giraffe () in Ruaha National Park, Tanzania. We found that GSD lesions altered normal walking gait kinematics (i.e., decreased walking speed and increased stride duration) largely irrespective of lesion severity or number of limbs affected. Impaired movement due to GSD could negatively impact foraging efficiency, dispersal, and predator susceptibility. Given that wildlife skin diseases are predicted to become more prevalent with climate change, examinations of their sublethal effects, in addition to their effects on mortality, are required to better understand long-term ramifications.
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http://dx.doi.org/10.1002/ece3.71774 | DOI Listing |
J Cosmet Dermatol
September 2025
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing, People's Republic of China.
Background: In recent years, the problem of female alopecia has been increasing and has shown a trend toward youthfulness. However, there are fewer studies on young female alopecia in the existing literature.
Aim: We aimed to study the possible causes of hair loss in young Chinese females aged 18-35 with oily scalps.
Ann Rheum Dis
September 2025
Department of Pediatrics, Division of Rheumatology, University of Michigan, Ann Arbor, MI, USA.
Objectives: Juvenile dermatomyositis (JDM) is a heterogeneous autoimmune condition needing targeted treatment approaches and improved understanding of molecular mechanisms driving clinical phenotypes. We utilised exploratory proteomics from a longitudinal North American cohort of patients with new-onset JDM to identify biological pathways at disease onset and follow-up, tissue-specific disease activity, and myositis-specific autoantibody (MSA) status.
Methods: We measured 3072 plasma proteins (Olink panel) in 56 patients with JDM within 12 weeks of starting treatment (from the Childhood Arthritis and Rheumatology Research Alliance Registry and 3 additional sites) and 8 paediatric controls.
Anal Chim Acta
November 2025
Department of Breast Surgery, General Surgery Center, First Hospital of Jilin University, Changchun, PR China. Electronic address:
Background: Breast-conserving surgery (BCS) is the primary surgical approach for patients with breast cancer. The accurate determination of surgical margins during BCS is critical for patient prognosis; however, time constraints and limitations in current pathological techniques often prevent pathologists from performing this assessment intraoperatively. The inability to reliably assess margins during surgery can lead to incomplete tumor removal and the need for additional surgeries.
View Article and Find Full Text PDFJ Hepatol
September 2025
Department of Neonatal Surgery, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China. Electronic address:
Background And Aims: Biliary atresia (BA) is a severe neonatal cholangiopathy characterized by progressive inflammation and fibrosis. We aimed to systematically investigate BA pathology using integrated multi-omics.
Methods: Multi-omics integration of BA and control livers revealed sphingolipid dysregulation.
Lancet Rheumatol
September 2025
Service de Médecine interne et polyvalente, Centre Hospitalier du Haut-Anjou, Château-Gontier, France; Université d'Angers, Inserm, CNRS, MITOVASC, Equipe MitoLab, SFR ICAT, F-49000 Angers, France. Electronic address:
Infections are increasingly recognised as a major cause of morbidity and mortality in patients with vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic (VEXAS) syndrome. We conducted a systematic review to characterise the infectious burden of VEXAS syndrome and propose preventive strategies. We included 57 studies (813 patients) showing that infections in patients with VEXAS syndrome were frequent, severe in 40-60% of cases, and fatal in 6-15% of cases.
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