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J-GLOBAL ID:201402217255697537   Reference number:14A0171004

Brain White Matter Abnormality in a Newborn Infant with Congenital Adrenal Hyperplasia

先天性副腎過形成の新生児における脳白質異常
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Volume: 22  Issue:Page: 77-81 (J-STAGE)  Publication year: 2013 
JST Material Number: L4217A  ISSN: 0918-5739  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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Crinical medicine on endocrine system in general 
Reference (12):
  • 1. Migeon CJ, Wisniewski AB. Congenital adrenal hyperplasia owing to 21-hydoroxylase deficiency. Endocr Metabol Cl North Am 2001; 30: 193-206.
  • 2. Nass R, Heier L, Moshang T, Oberfield S, George A, New MI, et al. Magnetic resonance imaging in the congenital adrenal hyperplasia population: increased frequency of white-matter abnormalities and temporal lobe atrophy. J Child Neurol 1997; 12: 181-6.
  • 3. Verpillat P, Alpérovitch A, Cambien F, Besancon V, Desal H, Tzourio C. Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities. Neurology 2001; 56: 673-5.
  • 4. Merke DP, Fields JD, Keil MF, Vaituzis AC, Chrousos GP, Giedd JN. Children with classic congenital adrenal hyperplasia have decreased amygdala volume: potential prenatal and postnatal hormonal effects. J Clin Endocrinol Metab 2003; 88: 1760-5.
  • 5. Bergamaschi R, Livieri C, Uggetti C, Candeloro E, Egitto MG, Pichiecchio A, et al. Brain white matter impairment in congenital adrenal hyperplasia. Arch Neurol 2006; 63: 413-6.
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