منابع مشابه
The virtual cranio-facial patient project Le projet de patient virtuel dans le domaine cranio-facial
One of the research goals at the Craniofacial Virtual Reality Laboratory and the Integrated Media Systems Center at the University of Southern California is to build a virtual craniofacial patient from CT data, digital teeth models, and human jaw motion tracking. First, two different techniques to acquire three-dimensional soft-tissue representations will be presented. Then, automatic segmentat...
متن کاملCranio-facial Dysostosis in a Dorset Family.
Crouzon (1912), whose name has been given to the combination of developmental anomalies which he described as hereditary cranio-facial dysostosis, presented his first two cases to the Societe Medicale des H6pitals de Paris. The patients, a mother aged 29 years and her son aged 21 years, had a malformation of the cranial vault consisting of protrusion in the region of the bregma, widening transv...
متن کاملCranio-facial clefts in pre-hispanic America.
Among the representations of congenital malformations in Moche ceramic art, cranio-facial clefts have been portrayed in pottery found in Moche burials. These pottery vessels were used as domestic items during lifetime and funerary offerings upon death. The aim of this study was to examine archeological evidence for representations of cranio-facial cleft malformations in Moche vessels. Pottery d...
متن کاملDental and cranio-facial aspects of Williams Syndrome
Williams Syndrome is a rare genetic disorder caused by a hemizygote micro-deletion mapped to the long arm of chromosome 7.The main symptoms are a distinctive facial appearance, psychomotor retardation with friendly behaviour and cardiovascular malformations. This case report describes the anomalies of the cranio-facial complex and the cephalometric aspects which are characteristic of this syndr...
متن کاملA possible cranio-oro-facial phenotype in Cockayne syndrome
BACKGROUND Cockayne Syndrome CS (Type A - CSA; or CS Type I OMIM #216400) (Type B - CSB; or CS Type II OMIM #133540) is a rare autosomal recessive neurological disease caused by defects in DNA repair characterized by progressive cachectic dwarfism, progressive intellectual disability with cerebral leukodystrophy, microcephaly, progressive pigmentary retinopathy, sensorineural deafness photosens...
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ژورنال
عنوان ژورنال: Japanese journal of science and technology for identification
سال: 1997
ISSN: 1882-2827,1342-8713
DOI: 10.3408/jasti.2.45