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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...
保存先:
| 出版年: | BMJ Case Rep |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
2018
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| 主題: | |
| オンライン･アクセス: | 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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