Literature DB >> 26505706

Orbital Dysmorphology in Untreated Children with Crouzon and Apert Syndromes.

Antonio Jorge Forte1, Derek M Steinbacher, John A Persing, Eric D Brooks, Tom W Andrew, Nivaldo Alonso.   

Abstract

BACKGROUND: Orbital dysmorphology and midface retrusion are the hallmarks of Crouzon and Apert syndromes. The precise nature of this deficiency is not known.
METHODS: Untreated Crouzon and Apert syndrome patients and age- and sex-matched controls were included. Computed tomographic scans were digitized and reconstructed. Craniometric and volumetric data relating to the orbit were collected.
RESULTS: Thirty-one scans were included (control, n = 12; Crouzon; n = 9; Apert, n = 10). The mean age of the Apert group was 5.31 ± 5 years; Crouzon, 5.77 ± 2.7 years; and control, 6.4 ± 3.6 years. The bony orbit length was 12 percent shorter in Apert (p = 0.004) and 17 percent shorter in the Crouzon group when compared to controls (p < 0.0001). The bony orbital volume was 21 percent smaller in the Apert children (p = 0.0006) and 23 percent smaller in Crouzon when compared to controls (p = 0.003). Globe volume was 15 percent larger in Apert (p = 0.008) and 36 percent larger in the Crouzon group when compared to controls (p < 0.0001). Orbital soft-tissue volume was 19 percent less in the Apert group (p = 0.004) and 29 percent less in the Crouzon group (p = 0.001) when compared to controls.
CONCLUSIONS: A shortened bony orbit, decreased orbital and orbital soft-tissue volumes, and an increased volume of the globe were found in both conditions. Despite normal volume of the overall orbital contents, the contents are altered, and the bony orbit is shorter and holds less volume.

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Year:  2015        PMID: 26505706     DOI: 10.1097/PRS.0000000000001693

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  4 in total

1.  Computer tomography-based quantitative analysis of the orbital proptosis severity in infants with syndromic craniosynostosis: case-control study.

Authors:  Rosalinda Calandrelli; Fabio Pilato; Antonio Marrazzo; Luca Massimi; Marco Panfili; Concezio Di Rocco; Cesare Colosimo
Journal:  Childs Nerv Syst       Date:  2021-02-08       Impact factor: 1.475

2.  Facial Malformation in Crouzon's Syndrome Is Consistent with Cranial Base Development in Time and Space.

Authors:  Xiaona Lu; Antonio Jorge Forte; Rajendra Sawh-Martinez; Sarika Madari; Robin Wu; Raysa Cabrejo; Derek M Steinbacher; Michael Alperovich; Nivaldo Alonso; John A Persing
Journal:  Plast Reconstr Surg Glob Open       Date:  2018-10-01

3.  Classification of Subtypes of Apert Syndrome, Based on the Type of Vault Suture Synostosis.

Authors:  Xiaona Lu; Rajendra Sawh-Martinez; Antonio Jorge Forte; Robin Wu; Raysa Cabrejo; Alexander Wilson; Derek M Steinbacher; Michael Alperovich; Nivaldo Alonso; John A Persing
Journal:  Plast Reconstr Surg Glob Open       Date:  2019-03-20

4.  The Postoperative Morphometrics of Orbital and Maxillary Area for Craniosynostosis.

Authors:  Lijun Shi; Weimin Shen; Qingwen Gao; Liangliang Kong
Journal:  J Craniofac Surg       Date:  2019-10       Impact factor: 1.046

  4 in total

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