Background: The point at which "normal" asymmetry becomes "abnormal" can be defined by an aesthetic limit and a functional limit. The underlying causes are still not fully discovered; the etiology includes congenital disorders, acquired diseases, and traumatic and developmental deformities. Our purpose was to investigate the possible genetic liability in the transmissibility of the asymmetric traits, through an analysis developed by twofold approach: 1) exploring and recording the family history through the use of a specific questionnaire; and 2) examining differences in laterality between the patients and their corresponding parent by a facial analysis.
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