Volume 21 No 1 (2023)
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MULTIPLE FRENULA- A MARKER OF UNDERLYING GENETIC ANOMALY: REPORT OF A CASE OF ELLIS-VAN CREVELD SYNDROME
DIVYA S, URALA ARUN S, MISHRA DIVYA, PRASAD G LAKSHMI, JAHAGIRDAR ABHISHEK
Abstract
Most often during oral examinations, dentists encounter with abnormal attachments of the
frenum. These frenal attachments often go unexamined by the dentists during oral
examination. Frenal attachments are thin folds of mucous membrane that attach the lips to the
alveolar mucosa and underlying periosteum. However, the presence of multiple frenula can be
a feature of several inherited syndromes. Ellis-van Creveld (EvC) syndrome, also termed as
chondroectodermal dysplasia or mesoectodermal dysplasia is a rare inherited genetic disorder
mainly affecting the ectodermal components. The characteristic features of this syndrome
include multiple frenula, hypodontia, polydactyly, short stature, cardiac and skeletal anomalies.
This paper describes one such syndrome that was suspected based on the multiple frenula
noted on oral examination in a teenage girl and confirmed after noting the presence of other
co-existing abnormalities.
Keywords
frenum; multiple frenula; Ellis-van Creveld syndrome; genetic syndrome
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