Results 51 to 60 of about 5,517 (177)

Synostosis of the Proximal Tibiofibular Joint

Case Reports in Medicine, 2010
The incidence of synostosis of the proximal tibiofibular joint (TFJ) was assessed among 1029 patients examined for osteoarthritis of the knee in a 4-year period.
Nikolaos K. Sferopoulos
doaj   +1 more source

Anatomical Considerations of Costal Abnormalities with its Clinical Significance

Archives of Medicine and Health Sciences
Synostosis is an immobile joint created by the ossification of two bones. About 0.3% of ribs have synostosis, an unexpected radiographic finding.
B. F. Jazeela, Meera Jacob, Ashwini Shetty   +2 more
doaj   +1 more source

Predictive Role of Shoulder Imbalance and Residual C7PL–CSVL in Coronal Imbalance After Surgery for Severe and Rigid Scoliosis: A Retrospective Analysis

Orthopaedic Surgery, Volume 18, Issue 4, Page 641-653, April 2026.
The prevalence of coronal imbalance remained high in severe and rigid scoliosis. Postoperative shoulder imbalance and residual trunk shift could be used as predictors for ultimate coronal imbalance. The aggravation of coronal imbalance might be a compensation, trying to level the imbalanced shoulder and attain a truncal global balance.
Honghao Yang, Haoshuang Geng, Jie Wang, Jixuan Huang, Yiqi Zhang, Yunsheng Wang, Yangpu Zhang, Lijin Zhou, Yong Hai   +8 more
wiley   +1 more source

Molecular Landscape in Limb Anomalies: Diagnostic Yield and New Candidate Genes

Clinical Genetics, Volume 109, Issue 3, Page 424-436, March 2026.
In 132 individuals with limb anomalies, diagnostic yield was 36% (47/132), including 25 novel variants, three cases with new phenotypes, and two candidate loci, HOXA11 and a small 2q31.1 deletion. Mouse data and exome‐wide analysis, key in identifying the candidate loci, represent an important opportunity for gene discovery.
Akram Mokhtari, Jade Charbonneau, Valancy Miranda, Khadijé Jizi, Marie‐Ange Delrue, Patricia Egerszegi, Isabelle Thiffault, Philippe M. Campeau   +7 more
wiley   +1 more source

Ertl surgery on the short fibula stump after war injury

Medicinski Glasnik
Aim To propose a new technique of Ertl-type surgery for significantly shortened and valgus deviated fibula stump. Methods We present the case of a 26-year-old patient who underwent reamputation surgery to replace a significantly shortened fibula ...
Viktor Shevchuk, Yurii Bezsmertnyi, Olexander Bezsmertnyi, Olexander Branitsky   +3 more
doaj   +1 more source

The Phenotypic Spectrum of Miller Syndrome: Insight From a French Cohort

Clinical Genetics, Volume 109, Issue 1, Page 188-193, January 2026.
This study expands the clinical spectrum of Miller syndrome by reporting novel features including preaxial defects, facial nevus simplex, and optic atrophy. It also includes the first patients with homozygous DHODH variants, emphasizing the importance of early diagnosis and the variability of presentations, from severe prenatal to mild adult phenotypes.
Marion Aubert Mucca, Perrine Brunelle, Martine Doco Fenzy, Clémence Vanlerberghe, Anne Dieux, Laura Feyereisen, Florence Jobic, Laurence Lode, Gwenael Le Guyader, Florence Petit, Elise Schaefer, Khaoula Zaafrane‐Khachnaoui, Alban Ziegler, Olivier Patat   +13 more
wiley   +1 more source

The influence of closed sutures on cranial morphology in Apert and Crouzon syndromes: A quantitative analysis

Journal of Anatomy, Volume 248, Issue 1, Page 40-52, January 2026.
This quantitative study identified distinct cranial vault morphologies in Apert and Crouzon syndromes, with a larger anterior fossa in Apert and high variability in Crouzon, reflecting different patterns of suture closure. Abstract Craniosynostoses are congenital conditions characterized by premature suture fusions, altering skull growth and ...
Ombline Delassus, Lyza Ben Bouazza, Adèle Rohée Traoré, Mathieu Uguen, Nathalie Boddaert, David Germanaud, Jean‐François Mangin, Giovanna Paternoster, Maxime Taverne, Roman Hossein Khonsari   +9 more
wiley   +1 more source

A Novel Approach to Study Cranial Shape in Children with Normal and Sagittal Synostosis: An Application of Geometric Morphometrics

Neurologia Medico-Chirurgica
To provide appropriate treatment, neurosurgeons and pediatricians must understand the chronological changes of the cranial morphology in normal children and the differences between normal and sagittal synostosis children. However, this issue has remained
Tadashi MIYAGAWA, Akira YAMAURA
doaj   +1 more source

A Novel MAP3K7 Variant Causing Loss of Function Identified in a Family With Cardiospondylocarpofacial Syndrome: Functional Validation and Molecular Insights

Human Mutation, Volume 2026, Issue 1, 2026.
Mitogen‐activated protein kinase kinase kinase 7 (MAP3K7), also known as transforming growth factor‐β–activated kinase 1 (TAK1), is a widely expressed kinase that plays a crucial role in various cellular processes variants in the MAP3K7 gene have been implicated in two distinct genetic disorders: frontometaphyseal dysplasia Type 2 (FMD2) and ...
Ting Zhu, Jiamin Shi, Jia Li, Tingmin Zhou, Xinru Fu, Fengzhen Xu, Chuangjie Gu, Danping Wang, Ruiting Wu, Li Liu, Jingling Shen, Dan Wang, Harleen Khatra   +12 more
wiley   +1 more source

Early treatment of congenital syngnathia. A case report

Journal of Pediatric and Neonatal Individualized Medicine, 2018
Congenital syngnathia is a rare malformation. The synechia or synostosis of the maxilla and the mandible may be partial or complete and also be associated with other malformations.
Eduardo Alfredo Duro, Stella Maris Benitez, Albano del Cristo Barreto Paternina   +2 more
doaj   +1 more source