Similar Diseases
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Results for Query ‹ Hypervalinemia medication ›
Hypervalinemia – Abstract
Hypervalinemia, also called valinemia or valine transaminase deficiency, is a rare autosomal recessive metabolic disorder in which urinary and serum levels of the branched-chain amino acid valine are elevated, without related elevation of the branched-chain amino acids leucine and isoleucine. It is caused by a deficiency of the enzyme valine transaminase.
Hypervalinemia – Characteristics
Presenting in infancy, symptoms include lack of appetite, vomiting, dehydration, hypotonia and failure to thrive.