Evidence map›Paper›PMID 42699920›Full record

ArticleInternational journal of surgery case reports2026

C2-C3 anterolisthesis with myelopathy in a toddler with Charcot-Marie-Tooth disease: a rare case and review of syndromic pediatric C2-C3 instability.

Sadegh Bagherzadeh, Faramarz Roohollahi, Sara M Hartnett, Puya Alikhani, Zohreh Habibi, Mohsen Rostami

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In one paragraph

Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sadegh BagherzadehDepartment of Neurosurgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0009-0000-1545-9218
Faramarz RoohollahiDepartment of Neurosurgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.ORCID https://orcid.org/0000-0001-7994-1097
Sara M HartnettDepartment of Neurosurgery, Brain and Spine, University of South Florida, Morsani College of Medicine, Tampa, FL, USA.
Puya AlikhaniDepartment of Neurosurgery, Brain and Spine, University of South Florida, Morsani College of Medicine, Tampa, FL, USA.
Zohreh HabibiDepartment of Neurosurgery, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Mohsen RostamiDepartment of Neurosurgery, Brain and Spine, University of South Florida, Morsani College of Medicine, Tampa, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and importance: Cervical instability and myelopathy are rare in young children and are frequently overlooked, particularly in those with syndromic or neuromuscular disorders, in which motor delay may be misattributed to the underlying condition. Reported cases of C2-C3 instability are extremely uncommon and have primarily been associated with syndromic diagnoses such as Down syndrome and achondroplasia. Recognizing treatable cervical pathology early is essential to prevent progressive neurological injury. Case presentation: We describe the first reported case of C2-C3 anterolisthesis and instability in a 22‑month‑old girl with Charcot-Marie-Tooth (CMT) disease, who was initially labeled as having cerebral palsy due to motor delay. Advanced imaging revealed congenital cervical anomalies, C2-C3 anterolisthesis, and significant spinal cord compression. The patient underwent surgical decompression with C1-C3 posterior fusion. Following surgery, she demonstrated progressive neurological and motor improvement. Clinical discussion: Although C2-C3 instability is exceedingly rare, the available literature indicates that it occurs most often in association with syndromic conditions and typically responds well to surgical fusion. This case reinforces the importance of considering cervical spine pathology in children with unexplained motor deficits, even when a syndromic diagnosis such as CMT is present. Early imaging and timely intervention can dramatically alter the clinical trajectory and prevent long-term disability. Conclusion: This case highlights the need for careful evaluation of cervical spine instability in pediatric patients with motor delay. Neurosurgeons should avoid prematurely attributing deficits to cerebral palsy or underlying syndromic disorders and should maintain a high index of suspicion for potentially reversible cervical pathology. Early diagnosis and surgical treatment can lead to substantial neurological recovery.

Indexed as

cervical instabilitycervical subluxationmyelopathy

Identifiers

PMID42699920
PMCPMC13544818

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.