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MCT8 Deficiency: Extrapyramidal Symptoms and Delayed Myelination as Prominent Features.

Authors :
Tonduti, Davide
Vanderver, Adeline
Berardinelli, Angela
Schmidt, Johanna L.
Collins, Christin D.
Novara, Francesca
Genni, Antonia Di
Mita, Alda
Triulzi, Fabio
Brunstrom-Hernandez, Janice E.
Zuffardi, Orsetta
Balottin, Umberto
Orcesi, Simona
Source :
Journal of Child Neurology. Jun2013, Vol. 28 Issue 6, p792-797. 6p.
Publication Year :
2013

Abstract

Monocarboxylate transporter 8 (MCT8) deficiency is an X-linked disorder resulting from an impairment of the transcellular transportation of thyroid hormones. Within the central nervous system thyroid hormone transport is normally mediated by MCT8. Patients are described as affected by a static or slowly progressive clinical picture which consists of variable degrees of mental retardation, hypotonia, spasticity, ataxia and involuntary movements, occasionally paroxysmal. The authors describe the clinical and neuroradiological picture of 3 males patients with marked delayed brain myelination and in which the clinical picture was dominated by early onset nonparoxismal extrapyramidal symptoms. In one subject a novel mutation is described. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08830738
Volume :
28
Issue :
6
Database :
Academic Search Index
Journal :
Journal of Child Neurology
Publication Type :
Academic Journal
Accession number :
87598690
Full Text :
https://doi.org/10.1177/0883073812450944