Cranio-facial Dysostosis in a Dorset Family
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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...
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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...
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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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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...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1966
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.41.218.375