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   <subfield code="a">Scurvy hidden behind neuropsychiatric symptoms</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Margherita Estienne, Marianna Bugiani, Alberto Bizzi, Tiziana Granata]</subfield>
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   <subfield code="a">Approaching an uncommon disease may result in diagnostic delay even in patients with typical clinical features. In this respect, diseases related to nutritional deficiencies may represent a diagnostic challenge. We describe a 2.5-year-old child with typical features of scurvy, who was referred for autistic-like behavior and severe muscle weakness and pain in lower limbs. Extensive investigations for non-nutrition-related disorders were first performed, including a muscle biopsy showing a selective type II fibers hypotrophy. Scurvy was eventually considered, after recalling the child's peculiar dietary habits.</subfield>
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   <subfield code="a">Vitamin C</subfield>
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   <subfield code="a">Estienne</subfield>
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   <subfield code="u">Department of Pediatric Neuroscience, National Neurological Institute &quot;C. Besta”, via Celoria 11, 20133, Milan, Italy</subfield>
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