False Negatives at Neonatal Screening for Congenital Adrenal Hyperplasia in Two Siblings with 21 -Hydroxylase Deficiency.

SHINOHARA O; ISHIGURO H; SHINAGAWA T; KUBOTA C

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J-GLOBAL ID：200902157611793608 Reference number：99A0461609

False Negatives at Neonatal Screening for Congenital Adrenal Hyperplasia in Two Siblings with 21 -Hydroxylase Deficiency.

21-ヒドロキシラーゼ欠損症を有する2兄弟における先天性副腎過形成に関する新生児スクリーニングにおける偽陰性

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Material：
Volume： 45 Issue： 3 Page： 427-430 Publication year： Jun. 1998
JST Material Number： F0625A ISSN： 0918-8959 Document type： Article
Article type：短報 Country of issue： Japan (JPN) Language： ENGLISH (EN)

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Endocrine diseases

Reference (6)：

PANG, S. Microfilter paper method for 17α-hydroxyprogesterone radioimmunoassay: Its application for rapid screening for congenital adrenal hyperplasia. J Clin Endocrinol Metab. 1977, 45, 1003-1008
PANG, W. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Pediatrics. 1988, 81, 866-874
SUWA, S. Nationwide survey of neonatal mass-screening for congenital adrenal hyperpkasia in Japan. Screening. 1994, 3, 141-151
BALSAMO, A. Congenital adrenal hyperplasia: Neonatal mass screening compared with clinical diagnosis only inthe Emilia-Romagna region of Italy, 1980-1995. Pediatrics. 1996, 98, 362-367
CUTFIELD, WS. Newborn screening for congenital adrenal hyperplasia in New Zealand. J Pediatr. 1995, 126, 118-121

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