تقرير
A novel case of Horner syndrome as the presenting sign of craniosynostosis.
| العنوان: | A novel case of Horner syndrome as the presenting sign of craniosynostosis. |
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| المؤلفون: | Diklich N; Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida., Panneerselvam S; Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida., Perez NE; Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida., Falcone M; Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida., Cavuoto KM; Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida. Electronic address: kcavuoto@med.miami.edu. |
| المصدر: | Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus [J AAPOS] 2024 Apr; Vol. 28 (2), pp. 103851. Date of Electronic Publication: 2024 Feb 16. |
| نوع المنشور: | Case Reports |
| اللغة: | English |
| بيانات الدورية: | Publisher: Elsevier Inc Country of Publication: United States NLM ID: 9710011 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-3933 (Electronic) Linking ISSN: 10918531 NLM ISO Abbreviation: J AAPOS Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: [New York] : Elsevier Inc. Original Publication: St. Louis, MO : Mosby-Year Book, Inc., c1997- |
| مواضيع طبية MeSH: | Horner Syndrome*/etiology , Horner Syndrome*/complications , Craniosynostoses*/complications , Craniosynostoses*/diagnosis , Craniosynostoses*/surgery, Male ; Humans ; Child ; Anisocoria/diagnosis ; Anisocoria/etiology ; Skull ; Optic Nerve |
| مستخلص: | Craniosynostosis, the premature fusion of cranial sutures, can lead to distortion of skull shape and neurological dysfunction. We present a novel case of Horner syndrome as the presenting sign of craniosynostosis associated with elevated intracranial pressure. A 10-year-old boy presenting for strabismus follow-up was noted to have new-onset anisocoria, greater in the dark, and mild right upper eyelid ptosis. Apraclonidine testing was concerning for Horner syndrome. Neuroimaging demonstrated previously undiagnosed sagittal craniosynostosis with tortuous optic nerves and large cerebrospinal fluid spaces around both optic nerves. The patient was referred to neurosurgery and underwent a lumbar puncture with an opening pressure of 44 cm H (Copyright © 2024 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.) |
| تواريخ الأحداث: | Date Created: 20240218 Date Completed: 20240409 Latest Revision: 20240523 |
| رمز التحديث: | 20240523 |
| DOI: | 10.1016/j.jaapos.2024.103851 |
| PMID: | 38368924 |
| قاعدة البيانات: | MEDLINE |
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Full Text Finder | تدمد: | 1528-3933 |
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| DOI: | 10.1016/j.jaapos.2024.103851 |