<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="Case Report" dtd-version="1.0"><front><journal-meta><journal-id journal-id-type="pmc">iarjmcr</journal-id><journal-id journal-id-type="pubmed">IARJMCR</journal-id><journal-id journal-id-type="publisher">IARJMCR</journal-id><issn>2709-3220</issn></journal-meta><article-meta><article-id pub-id-type="doi">https://doi.org/10.47310/iarjmcr.2022.v03i02.004</article-id><title-group><article-title>Syringomielia Sub Occipital Decompressions With Arnold-Chiary Syndrome Type I: Case Report</article-title></title-group><contrib-group><contrib contrib-type="author"><name><given-names>PigurAgus</given-names><surname>Marwanto</surname></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><given-names>Hanis</given-names><surname>Setyono</surname></name></contrib></contrib-group><aff-id id="aff-a" /><abstract>Syringomyelia is a rare case with very varied clinical symptoms involving the motor, sensory and autonomic systems, which have a clinical symptom similar to other disorders of the spinal cord. This disorder is rare or following congenital abnormalities such as the Arnold-Chiari malformation. The management of this patient with surgery and medication according of clinical condition, causes and other supporting examinations.&amp;nbsp;</abstract></article-meta></front><body /><back /></article>