Literature DB >> 2043952

The neurology of endemic cretinism. A study of two endemias.

J P Halpern1, S C Boyages, G F Maberly, J K Collins, C J Eastman, J G Morris.   

Abstract

Endemic cretinism is the most severe manifestation of dietary iodine deficiency. Two forms of the syndrome are traditionally described: neurological and myxoedematous. Although this classification highlights the important neurological sequelae of the disorder it implies that myxoedematous cretins have an alternative mechanism. Further, the nature of the neurological deficit associated with both types of endemic cretinism has received scant attention in recent times considering that it remains a common disorder in many parts of the world. The nature and extent of the neurological deficit found in endemic cretinism was investigated in 104 cretins from a predominantly myxoedematous endemia in western China and in 35 cretins from central Java, Indonesia, a predominantly neurological endemia. We found a similar pattern of neurological involvement in nearly all cretins from both endemias, regardless of type (myxoedematous or neurological), and of current thyroid function. Hallmarks of the neurological features included mental retardation, pyramidal signs in a proximal distribution and extrapyramidal signs. Many patients exhibited a characteristic gait. This probably reflected pyramidal and extrapyramidal dysfunction, although joint laxity and deformity were important contributing factors. Other frequently encountered clinical features were squint, deafness, and primitive reflexes. Cerebral computerized tomography (CT) revealed basal ganglia calcification in 15 of 50 subjects. The presence of basal ganglia calcification was confined to cretins with severe hypothyroidism. Otherwise, cerebral CT scanning demonstrated only minor abnormalities which did not contribute to the localization of the clinical deficits. We conclude that the same neurological disorder is present in both types of endemic cretinism reflecting a diffuse insult to the developing fetal nervous system. These clinical findings support the concept of maternal and fetal hypothyroxinaemia, arising from severe iodine deficiency, as the primary pathophysiological event in endemic cretinism. Differences between the two types of cretinism may be explained by continuing postnatal thyroid hormone deficiency in the myxoedematous type, which results in impaired growth, skeletal retardation and sexual immaturity.

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Year:  1991        PMID: 2043952     DOI: 10.1093/brain/114.2.825

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  16 in total

Review 1.  Administration of iodized oil during pregnancy: a summary of the published evidence.

Authors:  F Delange
Journal:  Bull World Health Organ       Date:  1996       Impact factor: 9.408

Review 2.  Biomarkers of nutrition for development--iodine review.

Authors:  Fabian Rohner; Michael Zimmermann; Pieter Jooste; Chandrakant Pandav; Kathleen Caldwell; Ramkripa Raghavan; Daniel J Raiten
Journal:  J Nutr       Date:  2014-06-25       Impact factor: 4.798

3.  Early maternal hypothyroxinemia alters histogenesis and cerebral cortex cytoarchitecture of the progeny.

Authors:  Rosalía Lavado-Autric; Eva Ausó; José Victor García-Velasco; María del Carmen Arufe; Francisco Escobar del Rey; Pere Berbel; Gabriella Morreale de Escobar
Journal:  J Clin Invest       Date:  2003-04       Impact factor: 14.808

4.  X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene.

Authors:  Knut Brockmann; Alexandra M Dumitrescu; Thomas T Best; Folker Hanefeld; Samuel Refetoff
Journal:  J Neurol       Date:  2005-04-18       Impact factor: 4.849

Review 5.  Thyroid hormone transporters--functions and clinical implications.

Authors:  Juan Bernal; Ana Guadaño-Ferraz; Beatriz Morte
Journal:  Nat Rev Endocrinol       Date:  2015-05-05       Impact factor: 43.330

6.  Early effects of iodine deficiency on radial glial cells of the hippocampus of the rat fetus. A model of neurological cretinism.

Authors:  J R Martínez-Galán; P Pedraza; M Santacana; F Escobar del Ray; G Morreale de Escobar; A Ruiz-Marcos
Journal:  J Clin Invest       Date:  1997-06-01       Impact factor: 14.808

7.  Mild iodine deficiency during fetal/neonatal life and neuropsychological impairment in Tuscany.

Authors:  F A Aghini Lombardi; A Pinchera; L Antonangeli; T Rago; L Chiovato; S Bargagna; B Bertucelli; G Ferretti; B Sbrana; M Marcheschi
Journal:  J Endocrinol Invest       Date:  1995-01       Impact factor: 4.256

Review 8.  Access, availability, and infrastructure deficiency: The current management of thyroid disease in the developing world.

Authors:  Jane Fualal; Joel Ehrenkranz
Journal:  Rev Endocr Metab Disord       Date:  2016-12       Impact factor: 6.514

9.  Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesis.

Authors:  C M Sue; D S Crimmins; Y S Soo; R Pamphlett; C M Presgrave; N Kotsimbos; M J Jean-Francois; E Byrne; J G Morris
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-08       Impact factor: 10.154

10.  Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter.

Authors:  Noriyuki Namba; Yuri Etani; Taichi Kitaoka; Yasuko Nakamoto; Mariko Nakacho; Kazuhiko Bessho; Yoko Miyoshi; Sotaro Mushiake; Ikuko Mohri; Hiroshi Arai; Masako Taniike; Keiichi Ozono
Journal:  Eur J Pediatr       Date:  2007-09-25       Impact factor: 3.183

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