Cranio-facial Dysostosis and Malformations of Feet
نویسندگان
چکیده
منابع مشابه
Cranio-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 کاملMandibulo - Facial Dysostosis * by Allan
THE first recorded cases of this comparatively rare congenital anomaly were reported by Berry (1889), but it was not until 11 years later that Collins (1900) recognized that the condition occurred as a syndrome. Further cases in Great Britain have been described by Mann and Kilner (1943) and Johnstone (1943). The clinical picture varies considerably from case to case and atypical, incomplete an...
متن کاملMalformations of the Hands and Feet
Female, Hindoo, aged 40; not known to be hereditary; neither father nor mother, sisters, brothers, nor children, have the deformity. The thumb of the left hand was very broad, bulging out at the end of the first phalanx, and then narrowing to the root of the single normal nail. The metacarpal bone was single, but flattened at its distal extremity, and presented two articular surfaces, to which ...
متن کاملThe 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 کاملMandibulo-facial dysostosis. A familial study.
MANDIBULO-FACIAL dysostosis is the name given by Franceschetti and Zwahlen (1944) and Franceschetti and Klein (1949) to a complex of symptoms which together comprise a congenital oro-facial syndrome (Wildervanck, 1960). Franceschetti and Klein (1949) reviewed the literature and described the typical characteristics of the syndrome as follows: (1) Antimongoloid palpebral fissures with either a n...
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ژورنال
عنوان ژورنال: Journal of Medical Genetics
سال: 1964
ISSN: 1468-6244
DOI: 10.1136/jmg.1.2.112