Abstract
Background/importance
Gollop-Wolfgang complex is a rare skeletal dysplasia with only 200 cases reported in the literature. This disorder is usually associated with several extraosseous anomalies. This report describes the first case of a fatty filum terminale and a low-lying conus medullaris in a patient with this complex. A review of the current literature of the Gollop-Wolfgang complex accompanies this case, highlighting the documented extraosseous anomalies seen in this complex.
Clinical presentation
We report a case of an 18-month-old patient with Gollop-Wolfgang complex who underwent cord untethering with release of the filum terminale after extensive workup showed the presence of a dyssynergic bladder and radiological evaluation revealed a fatty filum terminale and low-lying conus medullaris.
Conclusion
Gollop-Wolfgang complex is a skeletal dysplasia usually associated with several extra skeletal anomalies. Our report describes the first case of a fatty filum terminale and low-lying conus medullaris in this complex, as well as provides an overview of the documented anomalies seen in this disorder. A multidisciplinary approach is recommended when treating these infants in order to ensure that occult manifestations of the complex are not missed.
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Cyril Tankam and Mallory R. Peterson performed the literature review, prepared the figures, and wrote the main manuscript. Yaw Tachie-Baffour, Samer Zammar, and Elias Rizk assisted in the literature review, preparation of the figures, and writing of the manuscript. All authors reviewed the manuscript and approved the document for submission.
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Tankam, C.S., Peterson, M.R., Tachie-Baffour, Y. et al. Fatty filum terminale and low-lying conus medullaris in Gollop-Wolfgang complex: a case report and review of literature. Childs Nerv Syst 39, 517–526 (2023). https://doi.org/10.1007/s00381-022-05679-1
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DOI: https://doi.org/10.1007/s00381-022-05679-1