Cleidocranial dysplasia in a Thai cadaver.

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dc.contributor.authorNetvichit, Siriluk
dc.contributor.authorPilakasiri, Kajee
dc.contributor.authorCharernwat, Boonsong
dc.date.accessioned2012-05-23T09:33:11Z
dc.date.available2012-05-23T09:33:11Z
dc.date.issued2012-01
dc.description.abstractA rare cleidocranial dysplasia or Marie-Santon syndrome1 was seen in a man who devoted his body for anatomical study of medical students in faculty of Medicine Siriraj Hospital. It was shown that there were typical bony anomalies of this disease in his body. According to his family history, he was diagnosed as cleidocranial dysplasia. Until now he had transferred these characteristics to his two next generations; two sons, one daughter and one nephew. This disorder might have a strong genetic inheritance.en_US
dc.identifier.citationNetvichit Siriluk, Pilakasiri Kajee, Charernwat Boonsong. Cleidocranial dysplasia in a Thai cadaver. Siriraj Medical Journal, 2012 Jan; 64(suppl): 96-97.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/138595
dc.language.isoenen_US
dc.source.urihttps://www.sirirajmedj.com/content_download.php?content_id=2657en_US
dc.subjectCleidocranial dysplasiaen_US
dc.titleCleidocranial dysplasia in a Thai cadaver.en_US
dc.typeArticleen_US
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