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The Christ-Siemens-Touraine syndrome, or anhidrotic ectodermal dysplasia, presents three principal signs: anhidrosis or hypohidrosis, hypotrichosis and anodontia or hypodontia. This syndrome is of particular interest to stomatologists and orthodontists because of the particular therapeutic problems raised by the anodontia and associated skeletal anomalies.(More)
Pierre Marie and Sainton syndrome, or cleido-cranial dysostosis is characterised by a triad: clavicular aplasia, delayed ossification of the fontanelles and sutures of the vault of the skull and hereditary transmission. To these may be added multiple dental inclusions - hence its interest in stomatology. The authors described a familial hereditary case(More)
Histoplasmosis is a deep mycosis which occurs in America and Africa. It is extremely rare in France. The case presented involves a male subject who had spent time in the French colonies of Africa and in Brazil. He presented with undiagnosed ulceration of the cheek, similar to that seen with cancer. Diagnosis was made on histology on one hand and on(More)
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