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Article

1H magnetic resonance spectroscopy in monocarboxylate transporter 8 gene deficiency.

The Journal of clinical endocrinology and metabolism - 1 May 2008

Sijens Paul E, Rödiger Lars A, Meiners Linda C, Lunsing Roelineke J

Abstract excerpt

CONTEXT: In monocarboxylate transporter 8 (MCT8) gene deficiency, a syndrome combining thyroid and neurological abnormalities, the central nervous system has not yet been characterized by magnetic resonance (MR) spectroscopy. OBJECTIVE: We studied whether the degree of dysmyelinization in MCT8 gene deficiency according to MR imaging (MRI) is coupled with abnormalities in brain metabolism. DESIGN: MRI and MR...

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Identifiers

PMID: 18319316
DOI: 10.1210/jc.2007-2441

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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