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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:BMJ Case Rep
Prif Awduron: Verma, Rajesh, Mehta, Mannan, Shettigar, Chetan, Singla, Shinu
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMJ Publishing Group 2018
Pynciau:
Rare Disease
Mynediad Ar-lein: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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