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Eur Rev Med Pharmacol Sci ; 9(1): 49-52, 2005.
Article in English | MEDLINE | ID: mdl-15850144

ABSTRACT

We report on eight cases of patients affected by KBG syndrome (KBG stands for the initials of the affected patients in the original report), a rare genetic disease, that we find only in 40 cases mentioned in the scientific literature. In this work we present the minimum diagnostic criteria of diagnosis due to identify the syndrome and a hypothesis of study for the research of the involved factors.


Subject(s)
Abnormalities, Multiple/physiopathology , Child , Child, Preschool , Dental Caries/physiopathology , Female , Humans , Male , Musculoskeletal Abnormalities/physiopathology , Pain/physiopathology , Syndrome , Tooth Diseases/etiology
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