Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 May 10;11(5):e4937.
doi: 10.1097/GOX.0000000000004937. eCollection 2023 May.

Orbital and Eyelid Characteristics, Strabismus, and Intracranial Pressure Control in Apert Children Treated by Endoscopic Strip Craniectomy versus Fronto-Orbital Advancement

Affiliations

Orbital and Eyelid Characteristics, Strabismus, and Intracranial Pressure Control in Apert Children Treated by Endoscopic Strip Craniectomy versus Fronto-Orbital Advancement

Jenny C Dohlman et al. Plast Reconstr Surg Glob Open. .

Abstract

Apert syndrome is characterized by eyelid dysmorphology, V-pattern strabismus, extraocular muscle excyclorotation, and elevated intracranial pressure (ICP). We compare eyelid characteristics, severity of V-pattern strabismus, rectus muscle excyclorotation, and ICP control in Apert syndrome patients initially treated by endoscopic strip craniectomy (ESC) at about 4 months of age versus fronto-orbital advancement (FOA) performed about 1 year of age.

Methods: Twenty-five patients treated at Boston Children's Hospital met inclusion criteria for this retrospective cohort study. Primary outcomes were magnitude of palpebral fissure downslanting at 1, 3, and 5 years of age, severity of V-pattern strabismus, rectus muscle excyclorotation, and interventions to control ICP.

Results: Before craniofacial repair and through 1 year of age, none of the studied parameters differed for FOA versus ESC treated patients. Palpebral fissure downslanting became statistically greater for those treated by FOA by 3 (P < 0.001) and 5 years of age (P = 0.001). Likewise, severity of palpebral fissure downslanting correlated with severity of V-pattern strabismus at 3 (P = 0.004) and 5 (P = 0.002) years of age. Palpebral fissure downslanting and rectus muscle excyclorotation were typically coexistent (P = 0.053). Secondary interventions to control ICP were required in four of 14 patients treated by ESC (primarily FOA) and in two of 11 patients initially treated by FOA (primarily third ventriculostomy) (P = 0.661).

Conclusions: Apert patients initially treated by ESC had less severe palpebral fissure downslanting and V-pattern strabismus, normalizing their appearance. Thirty percent initially treated by ESC required secondary FOA to control ICP.

PubMed Disclaimer

Conflict of interest statement

The authors have no financial interest to declare in relation to the content of this article. This study was supported by Heed Ophthalmic Foundation funds and the Children’s Hospital Ophthalmology Foundation Chair funds.

Figures

Fig. 1.
Fig. 1.
A, Angle of palpebral fissure downslanting was measured as the angle between the inner canthal distance line and the palpebral fissure length line (positive value if axis below the horizontal and negative if above). B, Temporal to nasal interpalpebral fissure height ratio was defined as the distance between the upper and lower eyelid at the temporal limbus divided by the distance between the upper and lower eyelid at the nasal limbus.
Fig. 2.
Fig. 2.
Preoperative and early and late postoperative photographs of patients treated by ESC (A–C) and FOA (D–F). Both patients have the SER 252 TRP mutation.

References

    1. Lu X, Forte AJ, Sawh-Martinez R, et al. . Anterior convex lateral orbital wall: distinctive morphology in apert syndrome. Br J Oral Maxillofac Surg. 2018;56:864–869. - PubMed
    1. Forte AJ, Steinbacher DM, Persing JA, et al. . Orbital dysmorphology in untreated children with Crouzon and Apert syndromes. Plast Reconstr Surg. 2015;136:1054–1062. - PubMed
    1. Dagi LR, MacKinnon S, Zurakowski D, et al. . Rectus muscle excyclorotation and V-pattern strabismus: a quantitative appraisal of clinical relevance in syndromic craniosynostosis. Br J Ophthalmol. 2017;101:1560–1565. - PubMed
    1. Cohen MM, Kreiborg S. A clinical study of the craniofacial features in Apert syndrome. Int J Oral Maxillofac Surg. 1996;25:45–53. - PubMed
    1. Riesel JN, Riordan CP, Hughes CD, et al. . Endoscopic strip craniectomy with orthotic helmeting for safe improvement of head growth in children with Apert syndrome. J Neurosurg Pediatr. 2022;29:1–8. - PubMed

LinkOut - more resources