{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,8]],"date-time":"2026-07-08T05:02:21Z","timestamp":1783486941925,"version":"3.55.0"},"reference-count":10,"publisher":"SAGE Publications","issue":"10","license":[{"start":{"date-parts":[[2005,10,1]],"date-time":"2005-10-01T00:00:00Z","timestamp":1128124800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Child Neurol"],"published-print":{"date-parts":[[2005,10]]},"abstract":"<jats:p>We report a family with X-linked mental retardation that has a novel mutation in the monocarboxylate transporter 8 ( MCT8) gene associated with a characteristic neurodevelopmental phenotype with early childhood hypotonia that progresses to spasticity and global developmental delays. Affected patients experience moderate to severe psychomotor delays and congenital hypotonia, develop a myopathic facies, have diminished muscle bulk and generalized muscle weakness, develop progressive spasticity and movement disorders, and have limited speech but alert, affable personalities. Acquired microcephaly and abnormal myelination on brain magnetic resonance imaging can be present. Normal monocarboxylate transporter 8 gene functioning appears to be necessary for normal thyroid-associated metabolism in neurons. Abnormal thyroid function tests appear to be a consistent finding in the absence of typical signs of thyroid dysfunction. Although the phenotype appears to be consistent, and although the neurotoxic effects of abnormal central and peripheral neuromuscular system thyroid metabolism might be partly or wholly responsible for the neurologic phenotype reported, the exact mechanism remains unclear. ( J Child Neurol 2005;20:852\u2014857).<\/jats:p>","DOI":"10.1177\/08830738050200101601","type":"journal-article","created":{"date-parts":[[2007,6,21]],"date-time":"2007-06-21T22:00:05Z","timestamp":1182463205000},"page":"852-857","source":"Crossref","is-referenced-by-count":79,"title":["X-Linked MCT8 Gene Mutations: Characterization of the Pediatric Neurologic Phenotype"],"prefix":"10.1177","volume":"20","author":[{"given":"Kenton R.","family":"Holden","sequence":"first","affiliation":[{"name":"Greenwood Genetic Center Greenwood, SC, Department of Neurosciences (Neurology) and Pediatrics Medical University of South Carolina, Charleston, SC,"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Oscar F.","family":"Zu\u00f1iga","sequence":"additional","affiliation":[{"name":"Department of Pediatric Endocrinology CEMESA, San Pedro Sula, Honduras"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melanie M.","family":"May","sequence":"additional","affiliation":[{"name":"Greenwood Genetic Center Greenwood, SC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Humberto","family":"Su","sequence":"additional","affiliation":[{"name":"Department of Neurology CEMESA, San Pedro Sula, Honduras"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marco R.","family":"Molinero","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Division of Pediatric Neurology, Hospital Escuela Materno-Infantil, Tegucigalpa, Honduras"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. Curtis","family":"Rogers","sequence":"additional","affiliation":[{"name":"Greenwood Genetic Center Greenwood, SC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charles E.","family":"Schwartz","sequence":"additional","affiliation":[{"name":"Greenwood Genetic Center Greenwood, SC"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2005,10,1]]},"reference":[{"key":"atypb1","unstructured":"Monocarboxylate transporter 8 deficiency. Online Mendelian Inheritance in Man (OMIM) 1996-2005. Available at: http:\/\/www.ncbi.nlm.nih.gov\/entrez\/query.fcgi?cmd=300523. Accessed May 2005."},{"key":"atypb2","doi-asserted-by":"publisher","DOI":"10.1086\/431313"},{"key":"atypb3","doi-asserted-by":"publisher","DOI":"10.1086\/380999"},{"key":"atypb4","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(04)17226-7"},{"key":"atypb5","first-page":"325","volume":"48","author":"Allan W.","year":"1944","journal-title":"Am J Ment Defic"},{"key":"atypb6","first-page":"454","volume":"47","author":"Schwartz CE","year":"1990","journal-title":"Am J Hum Genet"},{"issue":"1","key":"atypb7","first-page":"72","volume":"12","author":"Lenzner S.","year":"2004","journal-title":"Eur J Hum Genet"},{"key":"atypb8","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-005-0713-3"},{"key":"atypb9","first-page":"23","volume":"22","author":"Seaver LH","year":"2003","journal-title":"Greenwood Genet Cent"},{"key":"atypb10","unstructured":"Kaye EM: Disorders primarily affecting white matter, in Swaiman KF, Ashwal S, (eds): Pediatric Neurology, Principles and Practice, 3rd ed. St. Louis, Mosby, 1999, 849\u2014859."}],"container-title":["Journal of Child Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/08830738050200101601","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/08830738050200101601","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T20:31:59Z","timestamp":1777494719000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/08830738050200101601"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,10]]},"references-count":10,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2005,10]]}},"alternative-id":["10.1177\/08830738050200101601"],"URL":"https:\/\/doi.org\/10.1177\/08830738050200101601","relation":{},"ISSN":["0883-0738","1708-8283"],"issn-type":[{"value":"0883-0738","type":"print"},{"value":"1708-8283","type":"electronic"}],"subject":[],"published":{"date-parts":[[2005,10]]}}}