Harvard Catalyst Profiles

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Mandibulofacial Dysostosis

"Mandibulofacial Dysostosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)


This graph shows the total number of publications written about "Mandibulofacial Dysostosis" by people in Harvard Catalyst Profiles by year, and whether "Mandibulofacial Dysostosis" was a major or minor topic of these publication.
Bar chart showing 16 publications over 13 distinct years, with a maximum of 2 publications in 1991 and 2011 and 2014
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.