Results 31 to 40 of about 2,507 (167)
The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice [PDF]
Nearly every extracellular ligand that has been found to play a role in regulating bone biology acts, at least in part, through MAPK pathways. Nevertheless, much remains to be learned about the contribution of MAPKs to osteoblast biology in vivo. Here we
Zhai, Bo +33 more
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ABSTRACT Objectives To develop a deep learning‐based framework to automate sector classification of unerupted maxillary canines (UMCs), assessing its accuracy and reliability compared to human ones. Material and Methods One thousand five hundred twenty‐eight UMCs from digital panoramic radiographs (PRs) were selected using data from the Dental ...
Marzio Galdi +7 more
wiley +1 more source
Frictional Fitting Removable Partial Denture for Patients with Cleidocranial Dysostosis
This Text is brought to you for free and open access by the Faculty of Health & Wellness Sciences at Digital Knowledge. It has been accepted for inclusion in Tygerberg Dental Sciences by an authorized administrator of Digital Knowledge.Cleidocranial ...
Prinsloo, Handre
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Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders
Abstract Dental anomalies occur frequently in a number of genetic disorders and act as major signs in diagnosing these disorders. We present definitions of the most common dental signs and propose a classification usable as a diagnostic tool by dentists, clinical geneticists, and other health care providers.
Muriel de La Dure‐Molla +24 more
wiley +1 more source
A Comparative Study of Pycnodysostosis, Cleidocranial Dysostosis, Osteopetrosis and Acro-osteolysis [PDF]
A radiological study of cases of pycnodysostosis, osteopetrosis, cleidocranial dysostosis and acro-osteolysis revealed an interwoven relationship as regards the X-ray findings with numerous identical signs that these conditions had in common.
Wolpowitz, A. +3 more
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Multidisciplinary management of cleidocranial dysplasia [PDF]
Background: Cleidocranial dysplasia (CCD), also known as cleidocranial dysostosis or osteodental dysplasia, is an autosomal dominant disorder caused by a microdeletion defect in chromosome 6p21.
Chalala, Chimène +3 more
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An insight into the malocclusion of cleidocranial dysplasia [PDF]
Cleidocranial dysplasia (CCD), formerly known as Cleidocranial dysostosis,is a rare congenital disorder of bone that is characterised by aplasia of, or deficient, clavicular formation, delayed and imperfect ossification of the cranium, relatively short ...
Dawjee, Salahuddien M. +2 more
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Cleidocranial dysplasia: A report of two cases
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder that presents with skeletal dysplasia. It commonly presents with significant dental problems such as retention of multiple deciduous teeth, impaction or delay in eruption of permanent teeth,
D N Mehta, R V Vachhani, M B Patel
doaj +1 more source
Refining the ethics of preimplantation genetic diagnosis: A plea for contextualized proportionality
Abstract Many European countries uphold a ‘high risk of a serious condition’ requirement for limiting the scope of preimplantation genetic diagnosis (PGD). This ‘front door’ rule should be loosened to account for forms of PGD with a divergent proportionality.
Wybo Dondorp, Guido de Wert
wiley +1 more source
Cleidocranial Dysplasia: Report of Two Cases
Cleidocranial dysplasia constitutes a congenital disorder manifested primarily in the development of facial and cranial bones, as well as partial development or complete absence of the clavicles and problems also arise on the number and eruption of teeth.
Avinash Kshar, H R Umarji
doaj +1 more source

