Link to the University of Pittsburgh Homepage
Link to the University Library System Homepage Link to the Contact Us Form

Craniofacial phenotype in Cutis Laxa

Lorenchick, Christa (2014) Craniofacial phenotype in Cutis Laxa. Master's Thesis, University of Pittsburgh. (Unpublished)

[img]
Preview
PDF
Submitted Version

Download (1MB) | Preview

Abstract

Cutis laxa (CL) is a rare connective tissue disorder associated with mutations in extracellular matrix genes that leads to loose, redundant, lax skin and is often accompanied by cardiovascular, pulmonary, musculoskeletal or neurological complications. Literature suggests that individuals with CL have distinctive craniofacial features. Prior reports have been inconsistent and to date no quantitative, objective analysis of the craniofacial phenotype has been carried out on this population. To address this deficit, state-of-the-art 3-dimensional (3D) imaging was used to capture quantitative facial measurements in a sample of individuals with cutis laxa and compare the facial morphology of affected individuals to matched controls. The hypothesis that different forms of CL (acquired vs congenital) exhibit different craniofacial phenotypes was also tested. Subjects were recruited as part of the Genetics of Extracellular Matrix in Health and Disease Study and 3D images of the head and face were acquired using a 3DMD portable stereophotogrammetry system. Twenty-four facial landmarks were identified on each subject’s 3D facial image, and from these landmarks, a set of standard anthropometric facial measurements was calculated. These shape coordinates were then subjected to principal components analysis to quantify and compare the major aspects of facial shape variation within and among groups. Congenital CL showed marked narrowing and lengthening of the face and subjects with ELN mutations had the most severe facial phenotypes. The craniofacial shape did not correlate with the individual’s skin elasticity supporting the conclusion that the craniofacial phenotype of CL is primarily caused by altered craniofacial development rather than skin laxity. The public health significance of this study is that craniofacial dysmorphism can occur as a part of many genetic syndromes. This type of quantitative study can be applied to any genetic disease with a distinct craniofacial phenotype and may assist the development of accurate, objective, sensitive and specific diagnostic criteria.


Share

Citation/Export:
Social Networking:
Share |

Details

Item Type: University of Pittsburgh ETD
Status: Unpublished
Creators/Authors:
CreatorsEmailPitt UsernameORCID
Lorenchick, ChristaCHL174@pitt.eduCHL174
ETD Committee:
TitleMemberEmail AddressPitt UsernameORCID
Thesis AdvisorUrban, Zsolturbanz@pitt.eduURBANZ
Committee MemberGrubs, Robinrgrubs@pitt.eduRGRUBS
Committee MemberWeinberg, Sethsmwst46@pitt.eduSMWST46
Committee MemberMcConnell, Juliannjuliann.mcconnell@chp.edu
Date: 27 June 2014
Date Type: Publication
Defense Date: 2 April 2014
Approval Date: 27 June 2014
Submission Date: 7 April 2014
Access Restriction: 1 year -- Restrict access to University of Pittsburgh for a period of 1 year.
Number of Pages: 65
Institution: University of Pittsburgh
Schools and Programs: Graduate School of Public Health > Genetic Counseling
Degree: MS - Master of Science
Thesis Type: Master's Thesis
Refereed: Yes
Uncontrolled Keywords: Cutis Laxa; connective tissue disorder; 3D imaging
Date Deposited: 27 Jun 2014 21:41
Last Modified: 15 Nov 2016 14:18
URI: http://d-scholarship.pitt.edu/id/eprint/21063

Metrics

Monthly Views for the past 3 years

Plum Analytics


Actions (login required)

View Item View Item