Results 31 to 40 of about 161,435 (256)

Fibrous Dysplasia

, 2021
Presentation covering an overview of fibrous ...
Mays El-Dairi, MD
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Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source

A Mazabraud’s syndrome: the rare coexistence of fibrous dysplasia and intramuscular myxoma. A case repot [PDF]

Chirurgia Narządów Ruchu i Ortopedia Polska
Mazabraud’s syndrome is a rare, benign skeletal disorder characterized by the coexistence of fibrous dysplasia and intramuscular myxoma. Genetic factors have been implicated in its aetiology.
Ezel Yaltırık Bilgin, Elif Aktaş, Erkan Bilgin   +2 more
doaj   +1 more source

Intelligent Orthopedics: Machine Learning in Diagnosis of Bone Disease, Implants, and Bone Health Monitoring

Advanced Healthcare Materials, EarlyView.
Efficient recovery from traumatic or degenerative diseases is a great challenge, even after all the advancements in bone and cartilage regeneration. Machine learning (ML) algorithms have presented opportunities to enhance these aspects by accurately analyzing imaging data.
Maryam Kamaei, Hesam Mohammadi, Shamim Golafshan, Mojtaba Alehosseini, Mahsa Mohammadzadeh, Atefeh Golshirazi, Nasim Golafshan, Tatiane Eufrásio‐da‐Silva, Alireza Dolatshahi‐Pirouz, Gorka Orive   +9 more
wiley   +1 more source

Exophytic variant of maxillary fibrous dysplasia; Fibrous dysplasia protuberans [PDF]

, 2014
Fibröz displazi, normal kemik dokunun yerini fibröz doku içeren mineralize bir dokunun aldığı, gelişimsel, neoplastik olmayan bir kemik hastalığıdır. Direkt radyografi, bilgisayarlı tomografi ve manyetik rezonans görüntüleme, fibröz displazi tanısında ...
Paksoy, Yahya, Sivri, Mesut, Uysal, Emine, Erol, Cengiz, Koplay, Mustafa, Erdoğan, Hasan   +5 more
core   +1 more source

Intramedullary rod fixation of fibrous dysplasia without use of bisphosphonates

Journal of Children's Orthopaedics, 2013
Purpose Controversy exists regarding approach to treatment of pediatric patients with fibrous dysplasia. Methods We retrospectively reviewed medical records of seven patients who were treated at our institution for fibrous dysplasia by intramedullary rod
Greg Gaski, Dane Hansen, Leisel M. Willis, Gary D. Bos, John R. Kean   +4 more
doaj   +1 more source

Nonvascular autologous fibular cortical strut graft with internal fixation in monostotic fibrous dysplasia of femur neck- A case report

Journal of Orthopaedic Reports, 2022
Introduction: Fibrous dysplasia is a non-inheritable congenital disorder characterized by bone-forming expansile fibrous lesions that disrupt normal bone architecture.
Mitali Mokashi, Amit Kumar Yadav, Sangeet Gawhale, Farokh Wadia   +3 more
doaj   +1 more source

Fibrous dysplasia of Faciomaxillary region case reports and review of literature [PDF]

, 2012
This article discusses the author's experience in managing fibrous dysplasia of faciomaxillary region. Data was accumulated from 2005 – 2011. All these cases were managed by the author.Commonest bone involved by fibrous dysplasia was maxilla (Literature ...
Thiagarajan, Balasubramanian; Stanley Medical college
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Longitudinal Morphomolecular Monitoring of Head and Neck Carcinogenesis

Advanced Science, EarlyView.
A miniaturized endoscopic probe that integrates Raman spectroscopy and optical coherence tomography, enabling simultaneous molecular and structural imaging of living tissue, was developed. Applied longitudinally in a mouse model of head and neck cancer, the system tracks disease progression from precancerous lesions to invasive cancer.
Jianrong Qiu, Priyanka G. Bhosale, Vishal Kumar, Jeyrroy Gabriel, Shiyue Liu, Ciro Chiappini, Richard J. Cook, Mads S. Bergholt   +7 more
wiley   +1 more source

ADNP‐Related Helsmoortel–Van der Aa Syndrome: A Review of the Literature and Clinical Recommendations for Assessment and Monitoring

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT ADNP‐related Helsmoortel–Van der Aa syndrome (ADNP‐related HVDAS) is a single gene form of autism spectrum disorder (ASD) caused by pathogenic sequence variants in the activity‐dependent neuroprotective protein (ADNP) gene. In addition to ASD, ADNP‐related HVDAS is associated with a wide range of cognitive, behavioral, and physical health ...
Jarrett Fastman, Ana Kolevzon, Paige Siper, Tess Levy, Jeffrey M. Saland, Yitzchak Frank, Robert Rapaport, Kayla Kupietzky, William E. Bennett Jr, Bruce Gelb, Sandra Bedrosian Sermone, Alexander Kolevzon   +11 more
wiley   +1 more source