Calcif. Tissue Int. 2020 Feb 01
New Function of RUNX2 in Regulating Osteoclast Differentiation via the AKT/NFATc1/CTSK Axis.
Xin Y, Liu Y, Liu D, Li J, Zhang C, Wang Y, Zheng S
Cleidocranial dysplasia is an autosomal dominant skeletal disorder resulting from RUNX2 mutations. The influence of RUNX2 mutations on osteoclastogene ...
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Source: PubMed
Fetal Pediatr Pathol 2020 Jan 26
Molecular Genetics of Cleidocranial Dysplasia.
Motaei J, Salmaninejad A, Jamali E, Khorsand I, Ahmadvand M, Shabani S, Karimi F, Nazari MS, Ketabchi G, Naqipour F
Background: Cleidocranial dysplasia (CCD) is a genetic disorder with an autosomal dominant inheritance pattern. CCD characterized by abnormal clavicle ...
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Source: PubMed
Sudan J Paediatr
Cleidocranial dysplasia.
Kutilek S, Machytka R, Munzar P
We present a 4-year-old girl with persistent anterior fontanelle and narrow sloping shoulders. The X-ray imaging revealed widely open anterior fontane ...
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Source: PubMed
BMC Pediatr
Cleidocranial dysplasia with growth hormone deficiency: a case report.
Takaki N, Mori J, Matsuo S, Osamura T, Michigami T
Cleidocranial dysplasia (CCD) is a rare skeletal disorder with autosomal dominant inheritance that is characterized by hypoplastic clavicles, delayed ...
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Source: PubMed
Imaging Sci Dent
Case series of cleidocranial dysplasia: Radiographic follow-up study of delayed eruption of impacted permanent teeth.
Yeom HG, Park WJ, Choi EJ, Kang KH, Lee BD
This report describes 3 cases of cleidocranial dysplasia (CCD) and presents relevant findings on long-term follow-up radiographic images of impacted p ...
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Source: PubMed
