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Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation
Authors:K?v?lc?m Gücüyener   ?i?dem Seher Kasapkara  Leyla Tümer  Marcel M. Verbeek
Affiliation:Department of Pediatric Neurology, Gazi University Hospital, Ankara, Turkey;1.Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey;2.Department of Neurology and Laboratory Medicine, Alzheimer Center Nijmegen, Nijmegen, Netherlands
Abstract:Aromatic L-amino acid decarboxylase (AADC), a vitamin B6-requiring enzyme that converts L-dopa to dopamine and 5-hydroxytryptophan to serotonin. Deficiency of this enzyme results in developmental delay, muscular hypotonia, dystonia, involuntary movements, autonomic dysfunction, and oculogyric crises. We now report a 2-year-old Turkish boy with AADC deficiency confirmed by greatly reduced AADC activity in the plasma and by genetic studies. Mutation analysis revealed a homozygous mutation c.208C > T (p. His70Tyr) in exon 3 of the AADC gene which has not been described to date.
Keywords:Aromatic L-amino acid decarboxylase deficiency   case report   novel mutation
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