Improved precision of newborn screening for congenital adrenal hyperplasia using weight-adjusted criteria for 17-hydroxyprogesterone levels

Journal of Pediatrics

Volumn 130, Issue 1, 1997, Pages 128-133

  Allen, D B ^a   Hoffman, G L ^a   Fitzpatrick, P ^a   Laessig, R ^a   Maby, S ^a   Slyper, A ^a  

^a H4/448 CSC Pediatrics   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HYDROXYPROGESTERONE; STEROID 21 MONOOXYGENASE;

ARTICLE; COHORT ANALYSIS; CONGENITAL ADRENAL HYPERPLASIA; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; FOLLOW UP; HUMAN; LABORATORY DIAGNOSIS; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; NEWBORN; NEWBORN SCREENING; PRACTICE GUIDELINE; PRIORITY JOURNAL; STEROID 21 MONOOXYGENASE DEFICIENCY;

EID: 0030729272     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(97)70321-4     Document Type: Article

References (13)

1. WL Miller LS. Levine Molecular and clinical advances in congenital adrenal hyperplasia J Pediatr 111 1987 1 17
2. RM Lebovitz RM Pauli R. Laxova Delayed diagnosis in congenital adrenal hyperplasia Am J Dis Child 138 1984 571 573
3. S Pang S Kling RH Dobbins Illinois experience in newborn screening for congenital adrenal hyperplasia: a new guideline for follow-up approach HB Bradford WH Hannon BL Therrell Proceedings of the 7th National Neonatal Screening Symposium, Nov. 15 to 19, 1989. Washington (DC) 1990 157 161
4. DB. Allen Salt-wasting 21-hydroxylase deficiency detected by newborn screening in a nonvirilized female [abstract] Pediatr Res 35 1994 544
5. S Pang J Hotchness AL Drash LS Levine MI. New Microfilter paper method for 17-alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia J Clin Endocrinol Metab 45 1977 1003 1008
6. S Pang W Murphy SL Levine A pilot screening program for congenital adrenal hyperplasia in Alaska J Clin Endocrinol Metab 55 1982 413 420
7. S Pang A. Clark Newborn screening, prenatal diagnosis, and prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency Trends in Endocrinology and Metabolism 1990;July/Aug 300 306
8. S Pang A. Clark Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: newborn screening and its relationship to the diagnosis and treatment of the disorder Screening 2 1993 105 139
9. S Pang MA Wallace L Hofman Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency Pediatrics 81 1988 866 874
10. DB Allen GL Hoffman SL Maby AH. Slyper Improved precision of newborn screening for 21-hydroxylase deficiency congenital adrenal hyperplasia using weight-adjusted criteria for 17-hydroxyprogesterone levels [abstract] Pediatr Res 37 4 1995 84A
11. PW Speiser B Dupont P Rubinstein High frequency of nonclassical steroid 21-hydroxylase deficiency Am J Hum Genet 37 1985 650 667
12. WS Cutfield D. Webster Newborn screening for congenital adrenal hyperplasia in New Zealand J Pediatr 126 1995 118 121
13. HC. Thuline Advances in neonatal screening (Excerpta Medical International Congress Series.) 1987 Elsevier Amsterdam 301 321