Results 31 to 40 of about 219 (121)

Prognostic Factors for Postoperative Complications. An Aggregate Protocol for 10 Observational Studies From the Danish TRIPLE‐A Cohort of 1.2 Million Surgeries

Acta Anaesthesiologica Scandinavica, Volume 70, Issue 7, August 2026.
ABSTRACT Background Postoperative complications substantially increase morbidity, mortality and healthcare costs. Understanding prognostic factors is essential for risk stratification, targeted prevention strategies, and development of prediction models.
Anders Peder Højer Karlsen, Asta Prescott, Caroline Folkersen, Jens Laigaard, Atena Saito, Caroline Lando Klammer, Mik Wetterslev, Emil Ipsen Ørskov, Mathilde Fahrendorff, Rebecca Kiær, Helene Holm Laigaard, Nichlas Hovmand, Lars Hyldborg Lundstrøm, Sebastian Buhl Rasmussen, Anders Kehlet Nørskov, Markus Harboe Olsen   +15 more
wiley   +1 more source

Hereditary multiple osteochondromas in a child: a case report and discussion of postoperative complication management

Frontiers in Surgery
BackgroundThe pathogenesis of hereditary multiple exostoses is mainly related to genetic variants and often requires surgical resection when it causes clinical symptoms.
Haiting Jia, Yuting Wang, Tao Liu
doaj   +1 more source

Clinical and Genetic Spectrum of Filippi Syndrome: A Systematic Review of Published Case Reports and Case Series

Health Science Reports, Volume 9, Issue 7, July 2026.
ABSTRACT Background and Aims Filippi syndrome is a very rare autosomal recessive craniodigital disorder primarily caused by mutations in the gene CKAP2L, characterized by syndactyly, microcephaly, growth retardation, distinctive craniofacial features, and intellectual disability.
Muhammad Anas Faheem, Laraib Ghanghro, Ayesha Khan, Maryam Khalid, Salwa Bashir, Dania Iqbal, Adan Ali, Hussain Haider Shah, Sameer Abdul Rauf, Humaira Kalam   +9 more
wiley   +1 more source

Hereditary multiple exostoses and schizophrenia

Indian Journal of Human Genetics, 2008
I report a case of a patient who suffered schizophrenia and multiple exostoses and argue the possible role of EXT gene and nearly chromosomal loci in further genetic investigations related to schizophrenia.
openaire   +3 more sources

Ilizarov technique for the treatment of hereditary multiple exostoses: A case report

Asian Journal of Surgery
Mingwang zhou, Pengwei Zhang, Xiaotong Liu, Mingyuan Tan, Zhenhua Shi   +4 more
doaj   +3 more sources

Asymmetrical Steps: Osteomorphological and Metric Patterns of Cattle Phalanges to Determine Anatomical Position

International Journal of Osteoarchaeology, Volume 36, Issue 4, Page 1013-1025, July/August 2026.
ABSTRACT This study presents a reproducible framework for identifying the anatomical position of cattle phalanges, integrating both morphological and osteometric approaches for application to modern and zooarchaeological assemblages. The dataset comprises 1853 phalanges from 106 individuals with known and unknown phalangeal position representing ...
Audrey Crabbé, Willemien de Kock, Canan Çakırlar   +2 more
wiley   +1 more source

Hereditary Multiple Exostoses with Rare Ocular Finding: A Case Report

Journal of Current Ophthalmology
Purpose: To study rare ocular findings in a rare case of hereditary multiple exostoses (HME) and to study HME in one family. Methods: HME is an autosomal dominant genetic disease characterized by the presence of multiple exostoses (osteochondromas).
Shashi Tanwar, Nishtha Saini, Krutika Boriwal, Prashant Sharma   +3 more
doaj   +1 more source

A Case of Hereditary Multiple Exostoses: Role of FNAC in diagnosis [PDF]

Perspectives In Medical Research
Hereditary Multiple Exostoses (HME) is a rare autosomal dominant bone disease. It is characterized with numerous benign osteochondromas, which grow outward from the metaphyses of long bones.
Annu Nanda, Qury Sabita Mahapatra, Shalini Trivedi   +2 more
doaj   +1 more source

Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia

Clinical Genetics, Volume 110, Issue 1, Page 3-14, July 2026.
Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise, Benkirane‐Jessel Nadia, Anton Nicolas, Vandamme Thierry, Clauss François, Conzatti Guillaume   +5 more
wiley   +1 more source

Prosthodontic and Occlusal Management of a Patient With Facial Port‐Wine Stains: A Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This study aims to present the prosthetic rehabilitation of a patient affected by Port‐Wine Stain (PWS), a condition involving intraoral tissues that may pose challenges to removable prosthodontic treatment due to altered mucosal resiliency, pronounced hypersensitivity, and vascular fragility.
Ana‐Maria Condor, Daniela Cornelia Condor, Andreea Kui, Simona Iacob, Alexandra Tărchilă, Smaranda Buduru, Andrea Chisnoiu   +6 more
wiley   +1 more source