Results 71 to 80 of about 3,792 (182)

A Retinoid Antagonist Attenuates Bone Growth Inhibition Caused by Growth Plate Injury in Mice

Journal of Orthopaedic Research, Volume 43, Issue 10, Page 1724-1735, October 2025.
ABSTRACT Growth plate injury, which may trigger growth plate fusion or arrest, is a common occurrence in pediatric orthopaedics that can lead to angulation of the limb and limb length discrepancy. Growth plate injuries are currently treated palliatively, with surgical intervention when severe limb length discrepancy or angulation is found during follow‐
Masatake Matsuoka, Ningfeng Tang, Tian Hongying, Kenta Uchibe, Satoru Otsuru, Norimasa Iwasaki, Joshua M. Abzug, Motomi Enomoto‐Iwamoto, Masahiro Iwamoto   +8 more
wiley   +1 more source

Activin-dependent signaling in fibro/adipogenic progenitors causes fibrodysplasia ossificans progressiva

Nature Communications, 2018
Fibrodysplasia ossificans progressiva is a severe disorder characterized by heterotopic ossification, and is caused by mutations in ACVR1. Here, the authors show that expression of mutant ACVR1 in fibro/adipogenic progenitors recapitulates disease ...
John B. Lees-Shepard, Masakazu Yamamoto, Arpita A. Biswas, Sean J. Stoessel, Sarah-Anne E. Nicholas, Cathy A. Cogswell, Parvathi M. Devarakonda, Michael J. Schneider, Samantha M. Cummins, Nicholas P. Legendre, Shoko Yamamoto, Vesa Kaartinen, Jeffrey W. Hunter, David J. Goldhamer   +13 more
doaj   +1 more source

Diagnosis of Pediatric Myositis Ossificans Based on Cytomorphology and Molecular Analysis From FNAB Sample: A Case Report

Diagnostic Cytopathology, Volume 53, Issue 7, Page E138-E143, July 2025.
ABSTRACT Myositis ossificans (MO) is a benign soft tissue lesion, characterized by ectopic ossification due to inappropriate fibroblast differentiation, most commonly affecting skeletal muscles. It often occurs in young adults after muscle trauma, predominantly in male patients and very rarely in children. We describe the case of a previously healthy 3‐
Živa Ledinek, Milica Stefanović, Blaž Mavčič, Maja Česen Mazić, Ana Gazikalović, Daja Šekoranja, Simona Miceska, Veronika Kloboves Prevodnik   +7 more
wiley   +1 more source

Post‐COVID‐19 Exacerbation of a Stable Fibrous Dysplasia: A Case Report

Clinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT Fibrous dysplasia (FD) is a rare, benign fibro‐osseous lesion characterized by replacement of normal bone with extensive fibrous stroma due to abnormalities in osteoblast differentiation. After puberty and during adulthood, FD lesions usually become quiescent. However, some cases show signs of regrowth and reactivation.
Mohammed Taib Fatih, Mohammed Abdalla Mahmood, Mohammed Khalid Mahmood, Amanj Ismael Tahir, Handren Ameer Kurda, Mohammed Aso Abdulghafor, Balen Hamid Qadir, Zana Fuad Noori   +7 more
wiley   +1 more source

Fibrodysplasia Ossificans Progressiva: A Case Report

Journal of Orthopaedic Surgery, 2013
Fibrodysplasia ossificans progressiva or myositis ossificans is a rare disease characterised by bony deposits or the ossification of soft tissues. It transforms skeletal muscles, tendons, ligaments, fascia, and aponeuroses into heterotopic bony deposits ...
Anoop C Dhamangaonkar, Akhil A Tawari, Arvind B Goregaonkar   +2 more
doaj   +1 more source

Fibrodysplasia Ossificans Progressiva: treatment and oral considerations [PDF]

, 2018
Treball Final de Grau d'Odontologia, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Curs: 2017-2018, Director: Francesc Ventura PujolFibrodysplasia ossificans progressiva (FOP) is a rare disease with a worldwide prevalence of one ...
Gutiérrez Nava, María Gabriela
core  

ACVR1 Gene Mutation in Sporadic Korean Patients with Fibrodysplasia Ossificans Progressiva [PDF]

, 2009
Fibrodysplasia ossificans progressiva (FOP; OMIM 135100) is a rare but extremely disabling genetic disorder of the skeletal system, and is characterized by the progressive development of ectopic ossification of skeletal muscles and subsequent joint ...
Chin Youb Chung, Choi, Cohen, Connor, Crow, Dong Yeon Lee, Groppe, Hye Ran Lee, In Ho Choi, Janoff, Kaplan, Kaplan, Kaplan, Kitterman, Lin, Moon Seok Park, Nakajima, Shore, Shore, Tae-Joon Cho, Won Joon Yoo   +20 more
core   +2 more sources

Genetic Testing Utilization in the U.S. Registry for Childhood Interstitial and Diffuse Lung Diseases

Pediatric Pulmonology, Volume 60, Issue 4, April 2025.
ABSTRACT Introduction Childhood interstitial and diffuse lung diseases (chILD) comprise a diverse group of rare disorders. Identifying the underlying cause is crucial for treatment, prognosis, and estimating recurrence risk. The objective of this study was to assess the utilization of genetic testing for subjects enrolled in the United States National ...
Laura A. Voss, Rebekah J. Nevel, Jennifer A. Wambach, Lawrence M. Nogee, Robin R. Deterding, Alicia M. Casey, Michael G. O'Connor, Daniel I. Craven, Jane B. Taylor, Gail H. Deutsch, Jade B. Tam‐Williams, Lea C. Steffes, Steven K. Brennan, Maria T. Santiago, Sara C. Sadreameli, Andrea F. Heras, Michael R. Powers, Antonia P. Popova, Manvi Bansal, Aaron Hamvas, William A. Gower, Fernando Urrego, Lisa R. Young, for The ChILD Registry Collaborative   +23 more
wiley   +1 more source

A CASE OF FIBRODYSPLASIA OSSIFICANS PROGRESSIVA WITH PRIMARY AMENORRHEA

Khyber Medical University Journal, 2011
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant hereditary disorder affecting around one in two million people. It is characterized by heterotopic calcification in muscles, tendons, ligaments, membranes and aponeurosis. It is the
Ayesha zafar, Syed Asad Maroof, Zafar Ali   +2 more
doaj  

Fibrodysplasia ossificans progressiva: a comprehensive review [PDF]

Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder that causes heterotopic ossification of soft tissues, leading to abnormal bone growth in muscles, tendons, and ligaments.
A., Subhashini, R. V., Raveena, S., Tamilselvan   +2 more
core   +2 more sources