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Brown–Vialetto–Van Laere syndrome
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Medical condition
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Brown-Vialetto-Van Laere syndrome (BVVL), is a rare, progressive, inherited neurodegenerative disorder that most often manifests in infancy or early childhood. Since 2010, mutations in the SLC52A1, SLC52A2, or SLC52A3 genes, which encode riboflavin transporters, have been identified as the cause of BVVL. BVVL is now known as riboflavin...

Instance of
class of disease
Subclass of
autosomal dominant disease
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