Impact of Early Intervention with Triiodothyroacetic Acid on Peripheral and Neurodevelopmental Findings in a Boy with MCT8 Deficiency

Monocarboxylate transporter 8 (MCT8) deficiency is a rare genetic disorder characterized by peripheral thyrotoxicosis and severe cognitive and motor disability due to cerebral hypothyroidism. 3,3',5-triiodothyroacetic acid (Triac) was shown to improve peripheral thyrotoxicosis but data on neurodevel...

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Hauptverfasser:	Yağmur Ünsal, Gamze Hayran
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Pediatric Endocrinology and Diabetes Society 2024-03-01
Schriftenreihe:	JCRPE
Schlagworte:	mct8 deficiency allan-herndon-dudley syndrome triiodothyroacetic acid (triac) neurodevelopmental outcome t3 analogue
Online-Zugang:	https://jag.journalagent.com/z4/download_fulltext.asp?pdir=jcrpe&un=JCRPE-03164
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