Results 61 to 70 of about 2,661 (168)
Disostosis cleidocraneal. Estudio familiar
Revista Cubana de Medicina, 2002 Se estudió la disostosis cleidocraneal, enfermedad hereditaria del esqueleto que se transmite en forma autosómica dominante. Se analizaron 4 sujetos correspondientes a 3 generaciones de una misma familia.
Rafael Arocha Rodríguez +3 more
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Cone beam computed tomography and prosthodontic rehabilitation of cleidocranial dysostosis
, 2013 The aim of this study is to present a clinical case of a male patient with cleiodocranial dysostosis, in which the cone beam tomography was crucial in the decision making regarding the type of prosthetic rehabilitation to ...
Inês Côrte-Real +4 more
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Cleidocranial dysplasia: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2008 Cleidocranial dysplasias is an autosomal dominant disorder that presents with skeletal dysplasia. The dental manifestations are mainly delayed exfoliation of primary teeth and delayed eruption of permanent teeth, with multiple impacted supernumeraries ...
Hemalatha R, Balasubramaniam M
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Spondylothoracic and spondylocostal dysostosis. Hereditary forms of spinal deformity
, 1988 Two siblings with spondylothoracic dysostosis, and two siblings and three unrelated children with spondylocostal dysostosis are described. Both conditions are inherited and characterised by malformed thoracic and lumbar vertebrae.
JM Connor +3 more
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, 2013 Jarcho Levin syndrome is a rare genetic disorder characterized by multipl vertebral and costal anomalies at birth. Jarcho Levin syndrome includes two phenotypic groups: spondylothoracic dysostosis and spondylocostal dysostosis.
PERÇİN, FERDA EMRİYE +4 more
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Congenital Pseudoarthrosis of Clavicle: A Rare Diagnosis in Neonate [PDF]
Indian Journal of Neonatal Medicine and Research, 2017 Tapas Bandyopadhyay +4 more
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, 1970 Cleidocranial dysplasia (CCD) is a bone disorder with cranial malformations, dental abnormalities, clavicular hypoplasia or agenesis and narrow thorax which allows approximation ofshoulders in front of chest. We report a case of CCD and discuss&
Chavva, Sunanda +3 more
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, 2012 Pycnodysostosis is a rare genetic disorder and was first described in 1962 by Maroteaux and Lamy. The incidence of this anomaly is estimated to be 1.7 per 1 million births.
Yavuz, İbrahim +2 more
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Síndrome de Marie Sainton. Presentación de casos [PDF]
, 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.
Escudero Alemán, Raisa +2 more
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, 2010 Cleidocranial dysplasia is a rare autosomal dominant condition with generalized dysplasia of bone, characterized by delayed closer of cranial sutures, hypoplastic or aplastic clavicles, short stature, dental abnormalities and a variety of other skeletal ...
Paramez A, Dixit Ramakant, Dixit Kalpana
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