Rare case of Gordon Holmes syndrome

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 abnormaliti...

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Bibliographic Details
Published in:BMJ Case Rep
Main Authors: Verma, Rajesh, Mehta, Mannan, Shettigar, Chetan, Singla, Shinu
Format: Artigo
Language:Inglês
Published: BMJ Publishing Group 2018
Subjects:
Rare Disease
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6040515/
https://ncbi.nlm.nih.gov/pubmed/29954774
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2018-225638
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