The Proper Diagnostic Pathway of Gardner’s Syndrome: Role of the Dentist in the Early Detection of the Associated Systemic Pathologies
Gardner’s
syndrome, a variant of Familial Adenomatous Polyposis (FAP), is a genetic
disorder with highly penetrant autosomal-dominant transmission (80-100%). The
incidence of FAP is approximately 1:7500 births, while Gardner’s syndrome
occurs in 1:14000 births.
The first researcher reporting a clinical case characterized
by the presence of manifestations which could be ascribed to Gardner’s syndrome
was Fitzgerald in 1943, however, the combination of these signs was recognized
as a genetically determined syndrome only in 1953 by Gardner e Richards. This
disease is characterized by the following triad: Gastrointestinal polyposis,
with a 100 percent chance of malignant degeneration, other signs are bone
tumors, frequently located on maxillary and cranial bones, and lastly the soft
tissues tumors.
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