Art

J-GLOBAL ID：200902250069664324   Reference number：03A0505314

Mortality in Patients with Congenital 21-Hydroxylase Deficiency Diagnosed after the Introduction of a Newborn Screening Program in Japan

日本において新生児スクリーニングプログラム導入後に先天性21-ヒドロキシラーゼ欠損症と診断された患児の死亡率

Author (9)： OGAWA E (Tohoku Univ. School of Medicine, Sendai, JPN) ,  FUJIEDA K ,  TACHIBANA K ,  KUSUDA S ,  NISHI Y ,  OKADA T ,  SAISHO S ,  TAJIMA T ,  TANAKA T
Material： Clinical Pediatric Endocrinology  (Clin Pediatr Endocrinol)
Volume： 12  Issue： 1  Page： 19-23  Publication year： Jun. 2003 
JST Material Number： L4217A  ISSN： 0918-5739  Document type： Article
Article type： 原著論文  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *enzymoprivicness ,...
Semi thesaurus term： 副腎肥大

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JST classification (3)： Congenital diseases,deformities in general.  (GD03010V) ,  Metabolic diseases,nutritional diseases in general.  (GD05010J) ,  Crinical medicine on endocrine system in general  (GL01030B)

Reference (7)：

• 1. Suwa S. Nationwide survey of neonatal mass-screening for adrenal hyperplasia in Japan. Screening 1994; 3:141-51.
• 2. Jaaskelainen J, Voutilainen R. Long-term outcome of classical 21-hydroxylase deficiency: Diagnosis, complications and quality of life. Acta Paediatr 2000;89: 183-7.
• 3. Swerdlow AJ, Higgins CD, Brook CGD, Dunger DB, Hindmarsh PC, Price, DA, et al. Mortality in patients with congenital adrenal hyperplasia: A cohort study. J Pediatr 1998; 133:516-20.
• 4. Togashi T, Matsuzono Y, Narita M. Epidemiology of influenza-associated encephalitis-encephalopathy in Hokkaido, the northern most island of Japan. Pediatr Int 1997; 42:192-6.
• 5. Kawashima Y, Hanaki K, Kinoshita T, Sugimoto S, Tsukuda T, Nagaishi J, et al. Increased incidence of acute encephalopathy among patients with congenital adrenal hyperplasia in Japan: A nation-wide survey. Program 84th Annual Meeting of the Endocrine Society, San Francisco, USA, 2002: 486.

Terms in the title (6)： 日本 ,  新生児スクリーニング ,  21-ヒドロキシラーゼ欠損症 ,  診断 ,  患児 ,  死亡率