Results 91 to 100 of about 3,948 (205)
Expression of the IL-11 Gene in Metastatic Cells Is Supported by Runx2-Smad and Runx2-cJun Complexes Induced by TGFβ1. [PDF]
, 2015 In tumor cells, two factors are abnormally increased that contribute to metastatic bone disease: Runx2, a transcription factor that promotes expression of metastasis related and osteolytic genes; and IL-11, a secreted osteolytic cytokine.
Afzal +59 more
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Cleidocranial dysplasia: A rare case report
Journal of Medical Sciences, 2017 Cleidocranial dysplasia (CCD) is a rare autosomal dominant skeletal disorder, characterized by delayed closure of anterior fontanelle, absent or hypoplastic clavicles, dental problems, and short stature.
Priyanka Minocha +2 more
doaj +1 more source
Prevalence of impacted and supernumerary teeth in the North Indian population [PDF]
, 2014 Objective: Dental impaction is a very frequent problem. Supernumerary teeth, or hyperdontia, are the presence of additional teeth to the normal series in the either of the dentition.
Maheshwari, Sneha, Santosh, Patil
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Marie-Sainton syndrome. Case reports
Acta Médica del Centro, 2011 Marie-Sainton syndrome, also known as cleidocranial dysostosis, has a florid clinical picture dominated by changes in the clavicles and skull. Abnormalities in tooth eruption and dysmorphism are other distinctive features of this condition.
Reynaldo E. Delis Fernández +2 more
doaj
First and second branchial arch syndromes: multimodality approach [PDF]
, 2018 First and second branchial arch syndromes (BAS) manifest as combined tissue deficiencies and hypoplasias of the face, external ear, middle ear and maxillary and mandibular arches.
Gudinchet, François +6 more
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Mymensingh medical journal : MMJ, 2008 Cleidocranial dysplasia (CCD) is a disorder that affects mostly those bones which derived from endochrondal and intramembranous ossification, such as the cranium and the clavicles. CCD is present at a frequency of one in one million individuals. Over 500 cases have been reported.
B, Zabeen +5 more
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Cleidocranial dysplasia with hearing loss
Journal of Natural Science, Biology and Medicine, 2013 Cleidocranial dysplasia is an inherited skeletal anomaly that affects primarily the skull, clavicle, and dentition, which can occur spontaneously, but most are inherited in autosomal dominant mode. The skull findings are brachycephaly, delayed or failed closure of the fontanelles, presence of open skull sutures and multiple wormian bones with ...
Candamourty, Ramesh +3 more
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Chirurgia narzadow ruchu i ortopedia polska, 1980 Five sporadic cases of cleidocranial dysostosis are described. Besides the classical findings, the clinical and roentgenological evaluation showed bilateral macrodactily of the second toe, aplasia of the 12th rib and severe acetabular dysplasia. This features had not been previously reported in medical literature.
R, Fragoso +5 more
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South African Journal of Radiology, 2018 We present a case of traumatic rupture of the spleen in a man with cleidocranial dysplasia. The computed tomography imaging showed multiple low-grade lacerations of the spleen which initially led to conservative patient management. However, with clinical
Prema Mohandas +2 more
doaj +1 more source
Diagnostics Of Supernumerary Teeth In Orthodontic Relapse [PDF]
, 2019 Aim: increasing the effectiveness of diagnosis and further orthodontic-surgical treatment of various clinical forms of hyperdontia (supernumerary teeth) and preventing recurrence with the use of cone-ray computer tomography data in orthodontic practice ...
Bindiuhin, O. (Oleksii)
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