The forms

The MHC database documents all the information collected via the M-H-Center forms.

Information from the database may be presented as diagrams and tables describing aspects of orofacial manifestations in rare disorders. This web site presents a sample of the diagnoses with a list of relevant reports from the database. Please feel free to contact the Mun-H-Center for more information from the database.

The MHC database – a national database for documentation of orofacial manifestations in rare disorders

The aim of the database is to document, analyze and present orofacial findings collected through clinical observations and information from parents.

The MHC database was established in 1996, and is under constant development. In January 2008, 2231 individuals were registered in the database. Together they represent slightly more than 200 different rare disorders.