Results 71 to 80 of about 17,263 (169)

CT Characteristics of Osteolathyrism in a Pig Model of β‐Aminopropionitrile and Surgery‐Induced Aortic Aneurysm

Veterinary Radiology &Ultrasound, Volume 66, Issue 4, July 2025.
ABSTRACT Pigs are established animal models for translational research studies of aortic aneurysms in humans. A recent publication recommended adding oral treatment of β‐aminopropionitrile (BAPN) as a technique for enhancing surgically induced aortic aneurysm formation in pig models.
Jeryl Jones, Matt Breed, Guillermo Rimoldi, Naren Vyavahare, Ahmed Ali   +4 more
wiley   +1 more source

Characteristics of hip impingement syndrome in patients with multiple hereditary exostoses

BMC Musculoskeletal Disorders, 2021
Backgrounds This study aimed to investigate the characteristic deformities of the hip in multiple hereditary exostoses patients (MHE) and its association with the hip impingement syndrome.
Yeong-Seub Ahn, Sungmin Kim, Woo-Jong Kim, Jun-Hyuk Lim, Sung-Taek Jung   +4 more
doaj   +1 more source

Postcranial anomalies of Eocene freshwater pleurodiran and cryptodiran turtles from the Spanish Duero Basin

The Anatomical Record, Volume 308, Issue 6, Page 1659-1676, June 2025.
Abstract Testudines are one of the best‐represented taxonomic groups among the Paleogene taxa of the Duero Basin (Castile and Leon Autonomous Community, central Spain). Among them, Neochelys (Podocnemidide) and Allaeochelys (Carettochelyidae) are most abundant, allowing the population to be assessed for osteological anomalies.
Andrea Guerrero, Francisco Ortega, Santiago Martín de Jesús, Adán Pérez‐García   +3 more
wiley   +1 more source

Paediatric Hypotrichosis: A Clinical and Algorithmic Approach to Diagnosis

Australasian Journal of Dermatology, Volume 66, Issue 3, Page e109-e119, May 2025.
ABSTRACT Paediatric hypotrichosis is the clinical feature of paucity of hair arising congenitally or in early life with the presentation being that of the child whose hair is growing insufficiently. It is a hallmark finding of a diverse group of genodermatoses and sporadic disorders, presenting as either an isolated symptom or in association with ...
Neda So, Leona Yip, David Orchard
wiley   +1 more source

Longitudinal Observation of Changes in the Ankle Alignment and Tibiofibular Relationships in Hereditary Multiple Exostoses

Diagnostics, 2020
The longitudinal changes in the tibiofibular relationship as the ankle valgus deformity progresses in patients with hereditary multiple exostoses (HME) are not well-known.
Jae Hoo Lee, Chasanal Mohan Rathod, Hoon Park, Hye Sun Lee, Isaac Rhee, Hyun Woo Kim   +5 more
doaj   +1 more source

Ulnar lengthening for children with forearm deformity from hereditary multiple exostoses: a retrospective study from a tertiary medical center

BMC Pediatrics
Background Patients with hereditary multiple exostosis (HME) usually present with forearm deformity with or without radial head dislocation. Ulna lengthening has been proposed to address this condition.
Shuo Wang, Bomansaan Herman, Yiheng Wu, Ming Lei, Blessing Mutasa, Pan Hong, Jin Li   +6 more
semanticscholar   +1 more source

Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetuses

Prenatal Diagnosis, Volume 45, Issue 3, Page 276-286, March 2025.
Abstract Objective This study aimed to assess the detection rate of clinically significant results of prenatal exome sequencing (pES) in low‐risk pregnancies and apparently normal fetuses in non‐consanguineous couples. Methods A retrospective analysis of pES conducted at a single center from January 2020 to September 2023 was performed.
Michal Levy, Shira Lifshitz, Mirela Goldenberg‐Fumanov, Lily Bazak, Rayna Joy Goldstein, Uri Hamiel, Rachel Berger, Shlomo Lipitz, Idit Maya, Mordechai Shohat   +9 more
wiley   +1 more source

Genome scan reveals several loci associated with torus palatinus

Orthodontics &Craniofacial Research, Volume 28, Issue 1, Page 159-165, February 2025.
Abstract Objective Torus Palatinus (TP) is a common trait with an unclear aetiology. Although prior studies suggest a hereditary component, the genetic factors that influence TP risk remain unknown. The purpose of this study is to identify genetic variants associated with TP.
Myoung Keun Lee, Ahmed M. El Sergani, Noah Herrick, Rebecca M. Green, Carmencita Padilla, Carmen J. Buxó, Ross E. Long, Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton, Lina M. Moreno Uribe, Wasiu L. Adeyemo, Azeez Butali, Mary L. Marazita, John R. Shaffer, Seth M. Weinberg   +14 more
wiley   +1 more source

Hereditary Multiple Exostoses: Clinical, Molecular and Radiologic Survey in 9 Families

Prague Medical Report, 2017
Hereditary multiple exostoses (HME) represents a heterogeneous group of diseases often associated with progressive skeletal deformities. Most frequently, mutations in EXT1 and EXT2 genes with autosomal dominant inheritance are responsible for HME. In our
Karel Medek, Jiří Zeman, Tomáš Honzík, Hana Hansíková, Štěpánka Švecová, Kamila Beránková, Vendula Kučerová Vidrová, Miloslav Kuklík, Jiří Chomiak, Markéta Tesařová   +9 more
doaj   +1 more source

Analysis of a Series of 26 Cases With Prenatal Skeletal Dysplasia via Multiplatform Genetic Detection

Molecular Genetics &Genomic Medicine, Volume 13, Issue 1, January 2025.
ABSTRACT Background Skeletal dysplasia (SD) represents a series of highly heterogeneous congenital genetic diseases affecting the human skeletal system. Refined genetic diagnosis is helpful for the accurate diagnosis and prognosis evaluation of SDs.
Li‐min Cui, Hua‐ying Hu, Xiao‐mei Zhai, Ming‐fei Qi, Yan‐ming Liu, Cong‐ying Han, Jing Zhang, Ming Shen, Yu‐lan Xiang, Wen‐qi Chen, Kai Yang, Dong‐liang Zhang, Huan‐xia Xing   +12 more
wiley   +1 more source