The Treatment of Cleidocranial Dysostosis (Scheuthauer-Marie-Sainton Syndrome), a Rare Form of Skeletal Dysplasia, Accompanied by Spinal Deformities: A Review of the Literature and Two Case Reports [PDF]
Case Reports in Orthopedics, 2018 Cleidocranial dysostosis is a skeletal dysplasia inherited in an autosomal dominant manner and may lead to complications such as scoliosis and kyphosis, concurrent with various orthopedic involvements.
Mehmet Bülent Balioğlu +3 more
doaj +3 more sources
Cleidocranial dysostosis: a case report with clinical illustration [PDF]
The Pan African Medical Journal, 2021 Cleidocranial Dysostosis or Dysplasia (CCD) is an infrequent clinical condition, with an autosomal dominant hereditary mode of inheritance. Triad lesions: multiple supernumerary teeth, partial or complete absence of the clavicles and open sagittal ...
Vanesa Villamil +3 more
doaj +2 more sources
Cleidocranial dysplasia: A rare case report
Journal of Pharmacy and Bioallied Sciences, 2023 Cleidocranial dysplasia (CCD) is a rare hereditary disease of unknown etiology which was previously known as cleidocranial dysostosis. It usually follows an autosomal dominant mode of transmission with no predilection of genre or ethnic group.
Akshay A Dhobley +3 more
doaj +2 more sources
A familial case of cleidocranial dysostosis presenting upper limb ischemia [PDF]
São Paulo Medical Journal, 2005 CONTEXT: Upper limb ischemia is not as common as lower limb ischemia but may cause severe impairment or disability if it is misdiagnosed. CASE REPORT: A case of a woman with cleidocranial dysostosis resulting in upper right limb ischemia is presented ...
Walter Campos Júnior +4 more
doaj +2 more sources
Delayed eruption of permanent dentition and maxillary contraction in patients with cleidocranial dysplasia: review and report of a family [PDF]
International Journal of Dentistry, Volume 2018, Issue 1, 2018., 2018 Introduction. Cleidocranial dysplasia (CCD) is an inherited disease caused by mutations in the RUNX2 gene on chromosome 6p21. This pathology, autosomal dominant or caused by a spontaneous genetic mutation, is present in one in one million individuals ...
Barbato, E. +5 more
core +3 more sources
Cleidocranial dysostosis [PDF]
BMJ Case Reports, 2015 Riddhi, DasGupta +3 more
europepmc +4 more sources
Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations [PDF]
J Appl Oral Sci, 2022 Cleidocranial dysplasia (CCD) is a skeletal disorder affecting cranial sutures, teeth, and clavicles, and is associated with the RUNX2 mutations. Although numerous patients have been described, a direct genotype–phenotype correlation for RUNX2 has been ...
Heerapanon, Thanakorn +5 more
core +3 more sources
Interdisciplinary Neurosurgery, 2022 Cleidocranial Dysplasia (CCD) or Cleidocranial dysostosis is a very rare, under-diagnosed pathology caused by a variable degree of expression of a dominant gene.
Juan Esteban Muñoz Montoya +6 more
doaj +1 more source
Advances in Oral and Maxillofacial Surgery, 2023 The diagnosis of Cleidocranial dysplasia is approached via clinical features, genetic testing, and imaging. CCD includes delayed or non-closure of cranial sutures the presence of bulging anterior fontanelle and multiple supernumerary teeth. We report two
Faisal Joueidi +4 more
doaj +1 more source
Congenital Pseudarthrosis of the Clavicle in Children: A Systematic Review
Children, 2022 (1) Background: Congenital pseudoarthrosis of the clavicle is a rare condition due to the failure of the union process of the ossification nuclei of the clavicle.
Alessandro Depaoli +7 more
doaj +1 more source