Results 51 to 60 of about 1,065 (180)
Updated EUROCAT guidelines for classification of cases with congenital anomalies
Birth Defects Research, Volume 116, Issue 2, February 2024.Abstract Background Precise and correct classification of congenital anomalies is important in epidemiological studies, not only to classify according to etiology but also to group similar congenital anomalies together, to create homogeneous subgroups for surveillance and research.
Jorieke E. H. Bergman +7 more
wiley +1 more source
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 +5 more
doaj
Cleidocranial Dysplasia: Report of Two Cases
Journal of Indian Academy of Oral Medicine and Radiology, 2010 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
Mesiodens preventing eruption of a permanent central incisor [PDF]
, 2005 A maxillary midline supernumerary tooth is the most common type of supernumerary tooth. We present a case of a mesiodens, preventing eruption of a permanent central incisor.
Azzopardi, Alexander +2 more
core
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
Advantages of cone beam computed tomography (CBCT) in the orthodontic treatment planning of cleidocranial dysplasia patients: a case report [PDF]
, 2011 Our aim was to discuss, by presenting a case, the possibilities connected to the use of a CBCT exam in the dental evaluation of patients with Cleidocranial Dysplasia (CCD), an autosomal dominant skeletal dysplasia with delayed exfoliation of deciduous ...
A Becker +32 more
core +3 more sources
Cementum analysis in cleidocranial dysostosis
Indian Journal of Dental Research, 2008 Objective: Cleidocranial dysostosis (CCD) is a skeletal disorder associated with dental anomalies such as failure or delayed eruption of permanent teeth and multiple impacted supernumerary or permanent teeth.
Manjunath K +4 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
core
Pyknodysostosis - Two Case Reports
Journal of Indian Academy of Oral Medicine and Radiology, 2004 Two cases with the typical features of Pyknodystosis have been described with characteristic clinical and radiographic features. The patients with this syndrome should be differentiated from other closely related syndromes as cleidocranial dysostosis and
Jigna S Shah, Sonal Thakkar, Shweta GoeI
doaj
A Comparative Study of Pycnodysostosis, Cleidocranial Dysostosis, Osteopetrosis and Acro-osteolysis [PDF]
, 2018 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.
Matisonn, A, Wolpowitz, A
core +2 more sources