Annals of Indian Academy of Neurology (Jan 2014)

Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation

  • Kivilcim Gucuyener,
  • Cigdem Seher Kasapkara,
  • Leyla Tumer,
  • Marcel M. Verbeek

DOI
https://doi.org/10.4103/0972-2327.132652
Journal volume & issue
Vol. 17, no. 2
pp. 234 – 236

Abstract

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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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