Dental management of a patient
with Wilson’s disease
Paulo Sergio da Silva Santos, DDS, MsC, PhD, Karin Sa Fernandes, DDS, MsC, PhD, Alexandre Fraige, DDS, PhD Marina Gallottini, DDS, MsC, PhD
Paulo Sergio da Silva Santos, DDS, MsC, PhD, Karin Sa Fernandes, DDS, MsC, PhD, Alexandre Fraige, DDS, PhD Marina Gallottini, DDS, MsC, PhD
Wilson’s disease (WD) is an autosomal recessive genetic disease, characterized
by the accumulation of copper in the body—primarily in the brain
and liver—due to defective biliary copper excretion by hepatocytes.
WD may manifest clinically as liver disease, neurologic symptoms, and
Kayser-Fleischer corneal rings. This article presents a case involving
a 43-year-old man who had WD prior to liver transplantation. Oral
examination revealed petechiae in the oral mucosa, poor oral hygiene,
periodontal disease, missing teeth, and several carious teeth. Patients
with WD may present systemic changes that affect dental care. Dental treatment prior to liver transplantation is recommended to eliminate the
oral foci of infection and control oral disease
General Dentistry May/June 2015
http://www.agd.org/media/271906/MJ15_GenDent.pdf#page=66