Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation |
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Authors: | K?v?lc?m Gücüyener ?i?dem Seher Kasapkara Leyla Tümer Marcel M. Verbeek |
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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 |
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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. |
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Keywords: | Aromatic L-amino acid decarboxylase deficiency case report novel mutation |
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