Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.

ABSTRACT: Allan-Herndon-Dudley syndrome was among the first of the X-linked mental retardation syndromes to be described (in 1944) and among the first to be regionally mapped on the X chromosome (in 1990). Six large families with the syndrome have been identified, and linkage studies have placed the gene locus in Xq13.2. Mutations in the monocarboxylate transporter 8 gene (MCT8) have been found in each of the six families. One essential function of the protein encoded by this gene appears to be the transport of triiodothyronine into neurons. Abnormal transporter function is reflected in elevated free triiodothyronine and lowered free thyroxine levels in the blood. Infancy and childhood in the Allan-Herndon-Dudley syndrome are marked by hypotonia, weakness, reduced muscle mass, and delay of developme

SUBMITTER: Schwartz CE 

PROVIDER: S-EPMC1226193 | biostudies-literature | 2005 Jul

REPOSITORIES: biostudies-literature