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Face shape of unaffected parents with cleft affected offspring: combining three‐dimensional surface imaging and geometric morphometrics
Authors:SM Weinberg  SD Naidoo  KM Bardi  CA Brandon  K Neiswanger  JM Resick  RA Martin  ML Marazita
Affiliation:S.M. Weinberg, K.M. Bardi, C.A. Brandon, K. Neiswanger, J.M. Resick, M.L. Marazita, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, PA, USA
S.D. Naidoo, Department of Plastic and Reconstructive Surgery, Washington University School of Medicine, St. Louis, MO, USA
R.A. Martin, Department of Pediatrics, School of Medicine, St. Louis University, St. Louis, MO, USA
M.L. Marazita, Department of Human Genetics, Graduate School of Public Health and Psychiatry and Department of Psychiatry, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA
Abstract:
Authors – Weinberg SM, Naidoo SD, Bardi KM, Brandon CA, Neiswanger K, Resick JM, Martin RA, Marazita ML Objective – Various lines of evidence suggest that face shape may be a predisposing factor for non‐syndromic cleft lip with or without cleft palate (CL/P). In the present study, 3D surface imaging and statistical shape analysis were used to evaluate face shape differences between the unaffected (non‐cleft) parents of individuals with CL / P and unrelated controls. Methods – Sixteen facial landmarks were collected from 3D captures of 80 unaffected parents and 80 matched controls. Prior to analysis, each unaffected parent was assigned to a subgroup on the basis of prior family history (positive or negative). A geometric morphometric approach was utilized to scale and superimpose the landmark coordinate data (Procrustes analysis), test for omnibus group differences in face shape, and uncover specific modes of shape variation capable of discriminating unaffected parents from controls. Results – Significant disparity in face shape was observed between unaffected parents and controls (p < 0.01). Notably, these changes were specific to parents with a positive family history of CL / P. Shape changes associated with CL / P predisposition included marked flattening of the facial profile (midface retrusion), reduced upper facial height, increased lower facial height, and excess interorbital width. Additionally, a sex‐specific pattern of parent‐control difference was evident in the transverse dimensions of the nasolabial complex. Conclusions – The faces of unaffected parents from multiplex cleft families displayed meaningful shape differences compared with the general population. Quantitative assessment of the facial phenotype in cleft families may enhance efforts to discover the root causes of CL /P.
Keywords:3D stereophotogrammetry  face shape  geometric morphometrics  non‐syndromic clefting  unaffected parents
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