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11  Articles
1 of 2 pages  |  10  records  |  more records»
AbstractTwo cases of mandibulofacial dystostosis are presented in order to describe the features associated with the condition. Computed tomography (CT) is frequently performed on these patients to aid in surgical planning. 3D volume rendering provides th... see more

AbstractScapuloiliac dysostosis, also known as pelvis-shoulder dysplasia and Kosenow syndrome, is a rare skeletal dysplasia described first by Kosenow et al. in 1970. The main components of the syndrome are varying degrees of bilateral iliac and scapular ... see more

Szczepkowska Aleksandra, Osica Piotr, Janas-Naze Anna. Aspekt chirurgiczny opieki nad pacjentem z dysplazja obojczykowo-czaszkowa – opis przypadku = Surgical aspect of patient care with cleidocranial dysplasia - case report. Journal of Education, Health a... see more

AbstractMucopolysaccharidosis (MPS) comprises a group of conditions associated with an abnormality in glycoprotein or mucopolysaccharides metabolism. Types of MPS identified are MPS I-H (Hurler's syndrome, gargoylism), MPS II (Hunter's syndrome), MPS III ... see more

Binder’s syndrome or maxillonasal dysostosis is a rare congenital condition that primarily affects the mid-face andsometimes the vertebrae. It was named after von Binder who described three cases of hypoplastic maxilla-nasalcomplex in 1962. It can either ... see more

Jesper Brandt Andersen & Niels W. Bruun: Tetralogy of Steno-Fallot and Bartholin-Patau syndrome. A heart malformation and a malformation syndrome first described by Danish anatomists in the seventeenth century.The heart malformation tetralogy of Steno-Fal... see more

Introduction: Treacher Collins syndrome, or mandibulofacial dysostosis, is a hereditary disorder and is manifested by craniofacial malformations. The incidence is close to one case per 40,000 live births, without relation to gender or race. The infant car... see more

Introduction: Treacher Collins syndrome, or mandibulofacial dysostosis, is a hereditary disorder and is manifested by craniofacial malformations. The incidence is close to one case per 40,000 live births, without relation to gender or race. The infant car... see more


1 of 2 pages  |  10  records  |  more records»