Results 51 to 60 of about 1,796 (161)

Clinical Spectrum of Cleidocranial Dysplasia: A Case Report

National Journal of Community Medicine, 2010
Background: The developmental anomaly involving skeleton and teeth is Cleidocranial dysplasia. It is an autosomal disorder with equal sex distribution.
P Sakhi, P Yadav, R Susmitha, A Chawla, CJ Yadav, J Gupta   +5 more
doaj  

Cone-beam computed tomography: An inevitable investigation in cleidocranial dysplasia

Contemporary Clinical Dentistry, 2015
Cleidocranial dysplasia is a heritable skeletal dysplasia and one of the most common features of this syndrome is multiple impacted supernumerary teeth.
Nandita S Gupta, Ajas A Gogri, Manasi M Kajale, Sonali G Kadam   +3 more
doaj   +1 more source

Pathways to enhancing prenatal diagnosis of skeletal dysplasias

Pregnancy, Volume 2, Issue 3, May 2026.
Abstract Skeletal dysplasias are a group of Mendelian disorders that variably alter the development of the musculoskeletal system and phenotypically range from mild short stature syndromes to severe perinatal or neonatal morbidity. Prenatal diagnosis of these conditions can be challenging due to the lack of precision with ultrasound imaging compared to
Michelle Joy Wang, Christina Jacobsen, Jennifer Arnold, Ronald J. Wapner, Deborah Krakow   +4 more
wiley   +1 more source

Melatonin Counteracts Mechanical Unloading‐Induced Bone Loss Through YTHDF3‐Mediated m6A Modification of Dapk2 mRNA

Journal of Pineal Research, Volume 78, Issue 3, May 2026.
ABSTRACT Disuse osteoporosis, a consequence of prolonged mechanical unloading, is characterized by bone loss and elevated fracture susceptibility. Although melatonin exhibits bone‑anabolic properties, its mechanistic role in the context of mechanical unloading remains elusive.
Quan Sun, Liqun Xu, Zhikui Li, Junfei Zhang, Xiran Zhao, Lijun Zhang, Xiaoyan Zhang, Jiangdong Zhao, Yingjun Tan, Luyao Wang, Ge Zhang, Zebing Hu, Shu Zhang, Fei Shi   +13 more
wiley   +1 more source

Pycnodysostosis With Papilledema and Isolated Low Parathyroid Hormone Levels in an Eight‐Year‐Old Girl: A Genetically Confirmed Case Report

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Pycnodysostosis is a rare autosomal recessive skeletal dysplasia resulting from pathogenic variants in the CTSK gene, which encodes cathepsin K, a lysosomal cysteine protease expressed in osteoclasts. Deficiency of this enzyme leads to defective bone resorption and generalized osteosclerosis.
Meghana Krishna Kesineni, Naveen Jagadish Kandregula, Sameer Kumar Majety, Yulia Alekseevna Pimenova, Bhargav Kadali, Vineeth Potluri, Prudhvi Lekkala   +6 more
wiley   +1 more source

Craniofacial features of cleidocranial dysplasia

Journal of Dental Sciences, 2017
Cleidocranial dysplasia (CCD) is an autosomal-dominant malformation syndrome affecting bones and teeth. The most common skeletal and dental abnormalities in affected individuals are hypoplastic/aplastic clavicles, open fontanelles, short stature ...
Chin-Yun Pan, Yu-Chuan Tseng, Ting-Hsun Lan, Hong-Po Chang   +3 more
doaj   +1 more source

Cleidocranial dysplasia: Case report and literature review

Kouqiang hemian waike zazhi, 2023
Cleidocranial dysplasia (CCD) is rare, which was usually found accidentally when they consulted a doctor due to oral problems. Clinically, it is necessary to improve relevant examinations and deal with oral and maxillofacial problems for such cases.
CHAI An, LEI Rongchang, QU Binbin, LI He, SHAO Qi, JIANG Zhisheng   +5 more
doaj   +1 more source

CLEIDOCRANIAL DYSPLASIA - A Case Report

Journal of Indian Academy of Oral Medicine and Radiology, 2003
Cleidocranial Dysplasia is a disorder of teeth, jaws and other bones of body which arise.>due to chromosomal abnormalities, (autosomal dominant disorder).
Altaf Hussain Chalkoo, Irfana
doaj  

Application of Artificial Intelligence in Detecting Dental Anomalies: Current Models, Imaging Modalities, and Future Directions

Health Science Reports, Volume 9, Issue 3, March 2026.
ABSTRACT Background and Aim As dental anomalies can significantly affect esthetic and function, early detection and diagnosis are crucial for treatment and minimizing potential negative effects. Artificial intelligence (AI) has emerged as a promising tool for the segmentation and detection of dental anomalies in number, morphology, size, position, and ...
Mobina Sadat Zarabadi, Zeynab Pirayesh, Shaghayegh Najary, Alireza Jafarzade Ghadimi, Mohammad Behnaz   +4 more
wiley   +1 more source

Runx2 Regulated Airway Homeostasis Is Disrupted in Asthma

The FASEB Journal, Volume 40, Issue 4, 28 February 2026.
Runt‐related transcription factor‐2 (RUNX2) expression and regulation of airway remodeling factors were examined in asthmatic and nonasthmatic airway smooth muscle (ASM) cells. Regulation by transforming growth factor‐β of active RUNX2 isoform translocation to the nucleus was absent in asthmatic ASM, while RUNX2 overexpression suppressed markers of ...
Junfei Wang, Alen Faiz, Qi Ge, Rob van de Velde, Theo Borghuis, Brian G. Oliver, Maarten van den Berge, Victor Guryev, Alan James, John G. Elliot, Andrew J. Halayko, Liang Dong, Anthony W. Ashton, Janette K. Burgess   +13 more
wiley   +1 more source