Young-onset cerebellar syndromes are quite interesting and challenging for treating clinicians. While dealing with such cases, a clinician should be aware of rare possible causes too. We report a rare case of Gordon Holmes syndrome-an autosomal recessive cerebellar ataxia with endocrinal abnormalities.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6040515 | PMC |
http://dx.doi.org/10.1136/bcr-2018-225638 | DOI Listing |
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