Ophthalmic considerations in patients with Pfeiffer syndrome

Abstract Purpose We report here a newborn male infant with striking features consistent with severe Pfeiffer syndrome type II, including cloverleaf skull deformity with pansynostosis, extreme proptosis, upper extremity contractures, broad big toes and thumbs with varus deviation and genetic mutation...

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Bibliographic Details
Published in:American journal of ophthalmology case reports 2016-07, Vol.2 (C), p.1-3
Main Authors: Clark, Jeremy D, Compton, Christopher J, Tahiri, Youssef, Nunery, William R, Harold Lee, Hui Bae
Format: Article
Language:English
Subjects:
Craniosynostosis
Exorbitism
Ophthalmology
Pfeiffer syndrome
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Summary:Abstract Purpose We report here a newborn male infant with striking features consistent with severe Pfeiffer syndrome type II, including cloverleaf skull deformity with pansynostosis, extreme proptosis, upper extremity contractures, broad big toes and thumbs with varus deviation and genetic mutation in the FGFR2 gene. The authors review the ophthalmic complications in Pfeiffer syndrome and discuss the unique surgical strategies used for obtaining adequate corneal coverage in these unique patients. Observations Ophthalmic considerations in Type 2 Pfeiffer Syndrome include vision loss secondary to increased intracranial pressure, and extreme proptosis as a result of orbitostenosis and midfacial retrusion. Our patient has undergone multiple ophthalmic/oculoplastic, neurosurgical, and midfacial surgeries as a result of corneal deterioration due to extreme exorbitism. Conclusions and importance It is important for ophthalmologists to be aware of the ophthalmic complications associated with patients with craniosynostosis syndromes. Our case identifies the importance of close communication between ophthalmology and plastic reconstructive surgery to help formulate the most successful plan in treating corneal decompensation and proptosis in Pfeiffer Syndrome patients.
ISSN:2451-9936
2451-9936
DOI:10.1016/j.ajoc.2016.04.001