Abstract

BackgroundAchondroplasia is the most common dwarfing disorder. It can result in a variety of sequelae, including neurologic complications, among which high cervical myelopathy is one of particular concern. However, some individuals with achondroplasia appear to have persistent signs by physical examination that, while they might suggest the presence of high cervical myelopathy, remain isolated, non-progressive and apparently benign. To document and quantify these apparently benign craniocervical signs (ABCS) a cohort of 477 individuals with achondroplasia was retrospectively analyzed and information regarding persistent neurologic features suggestive of high cervical myelopathy was recorded in a REDCap database.ResultsWithin this cohort, 151 individuals (31.7%) had neurologic examinations that were in some manner concerning.Of these, 46 (30.5% of the subpopulation) required cervicomedullary decompressive surgery. The remaining 105 had concerning signs by examination but no apparent evidence for clinically significant cervical myelopathy. Of those 105 individuals, 88 (83.8%; 18.4% of the entire population) remained neurologically intact throughout their follow-up, and without clinical sequelae.ConclusionsIt appears that many individuals with achondroplasia, if carefully examined, may demonstrate isolated, initially concerning signs suggestive of cervical myelopathy, but in the vast majority these are benign and do not indicate need for aggressive neurosurgical intervention. Further investigations may help to identify ways to differentiate these benign features from the less common but more problematic true myelopathic ones. We postulate that the “neurologic leftovers” may arise from temporally remote, subtle damage to the spinal cord at the craniocervical junction, which damage otherwise does not reach clinical relevance.

Highlights

  • Achondroplasia is the most common dwarfing disorder

  • At least 8–17% of individuals with achondroplasia will require cervicomedullary decompression surgery to minimize the effects of compression at the craniocervical junction [8–11]

  • 46 (30.5% of those with concerning examinations) were excluded from further consideration based on their need for cervicomedullary decompression surgery (Fig. 1)

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Summary

Introduction

Achondroplasia is the most common dwarfing disorder. It can result in a variety of sequelae, including neurologic complications, among which high cervical myelopathy is one of particular concern. To document and quantify these apparently benign craniocervical signs (ABCS) a cohort of 477 individuals with achondroplasia was retrospectively analyzed and information regarding persistent neurologic features suggestive of high cervical myelopathy was recorded in a REDCap database. Due to risks of compression at the craniocervical junction, all individuals with achondroplasia must undergo neurologic assessment including neurologic history and neurologic examination, imaging of the craniocervical junction (by computerized tomography or magnetic resonance imaging), and polysomnography shortly after initial diagnosis [3]. Distinguishing those with need for urgent surgical intervention from infants who display diagnosis-typical motor delays and axial hypotonia remains challenging. Criteria used in our clinics to determine if craniocervical decompression is warranted have been published previously [3, 7]

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