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The Anatomical Record, Volume 308, Issue 12, Page 3186-3196, December 2025.Examples from the graphic library depicting morphologies of interparietal bones, ossicles at lambda, mendosal sutures, and intrasutural ossicles. Abstract Due to its complex ossification during development, the superior region of the human occipital bone is a frequent site of supernumerary bones known as interparietal bones.
Melissa D. Clarkson +4 more
wiley +1 more source
Orthodontic Care of Cleidocranial Dysplasia Patients [PDF]
, 2015 Cleidocranial dysplasia (CCD) is a rare congenital deformity inherited as an autosomal genetic trait with the prevalence of 1:1,000,000. It is characterized by dental defomities such as retained primary teeth, presence of supernumerary teeth, skeletal ...
Rahime Burcu Nur +2 more
core +1 more source
Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders
Journal of Inherited Metabolic Disease, Volume 48, Issue 2, March 2025.ABSTRACT Phosphatidylinositol, a glycerophospholipid with a myo‐inositol head group, can form seven different phosphoinositides (PItds) by phosphorylation at inositol carbons 3, 4 and/or 5. Over 50 kinases and phosphatases participate in PItd metabolism, creating an interconnected PItd network that allows for precise temporal and spatial regulation of ...
Francis Rossignol +2 more
wiley +1 more source
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
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Case Reports in Dentistry, Volume 2025, Issue 1, 2025.Introduction: Gemination and fusion are rare developmental anomalies that can present significant diagnostic challenges. Due to the complexity of distinguishing between these conditions, the term “double tooth” is commonly employed in clinical practice.
Matteo Pellegrini +6 more
wiley +1 more source
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
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
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Dental treatment of patients with cleidocranial dysplasia: two case reports [PDF]
, 2023 Introduction: Cleidocranial dysplasia (CCD) is an autosomal dominant disorder, also referred to ascleidocranial dysostosis. The diagnosis is made on the basis of clinical and radiological findings and is confirmed through a genetic analysis ...
Dzhongova, Elitsa; Medical University of Varna +1 more
core +9 more sources
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
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Journal of Education, Health and Sport, 2016 Szczepkowska Aleksandra, Osica Piotr, Janas-Naze Anna. Aspekt chirurgiczny opieki nad pacjentem z dysplazją obojczykowo-czaszkową – opis przypadku = Surgical aspect of patient care with cleidocranial dysplasia - case report.
Aleksandra Szczepkowska +2 more
doaj +2 more sources