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Treatment with TRIAC in pediatric patients with MCT8.

Natalia GazekAna L FellerElisa VaianiIsabel Di PalmaAndrea SavranskyPablo RamirezRoxana MarinoNatalia Perez GarridoJuan M LazzatiViviana HerzovichNoelia Dujovne
Published in: Archivos argentinos de pediatria (2023)
Monocarboxylate transporters (MCTs) allow the cellular entry of thyroid hormones, especially into the central nervous system (CNS), where they are crucial for neurodevelopment. MCT8 deficiency results in the combination of hypothyroidism in the CNS and peripheral hyperthyroidism, characterized by elevated T3 levels. The only treatment currently available is 3,3',5-triiodothyroacetic acid (TRIAC), a thyroid hormone analogue aimed at improving peripheral thyrotoxicosis and preventing the progression of neurological impairment. Here we assess the clinical, imaging, biochemical, and genetic characteristics of 4 patients with MCT8 deficiency who have received TRIAC to date, the doses used, and the response to treatment.
Keyphrases
  • replacement therapy
  • high resolution
  • blood brain barrier
  • gene expression
  • mass spectrometry
  • dna methylation
  • smoking cessation