Nonclassical adrenal hyperplasia due to 21-hydroxylase-deficiency: Does genotyping predict the clinical manifestation?

Endocrine Research

Volumn 22, Issue 4, 1996, Pages 735-739

  L'Allemand, D ^a   Keller, E ^b   Hoeppner, W ^c   Serban, A ^d   Morel, Y ^d   Gruters A ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c UNIVERSITY OF HAMBURG   (Germany)

^d HÔPITAL DEBROUSSE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

STEROID 21 MONOOXYGENASE;

ADOLESCENT; ADRENAL HYPERPLASIA; CHILD; CLINICAL ARTICLE; CONFERENCE PAPER; ENZYME DEFICIENCY; FEMALE; GENE SEQUENCE; GENETIC DISORDER; GENOTYPE; HUMAN; INFANT; MALE; MUTATION; NEWBORN; NEWBORN SCREENING; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROMOTER REGION; SALT LOSING NEPHRITIS; SEQUENCE ANALYSIS; SOUTHERN BLOTTING;

EID: 0030459853     PISSN: 07435800     EISSN: None     Source Type: Journal    
DOI: 10.1080/07435809609043770     Document Type: Conference Paper

References (5)

1. Wilson RC, Mercado AB, Cheng KC, New MI. 1995 J. Clin. Endocrinol Metab 80:2322-2329
2. Morel Y, Murena M, Nicolina M, Carel JC, David M, Forest MG. 1992 Horm. Res. 37:13
3. Speiser PW, Dupont J, Zhu D, Serrat J, Buegeleisen M, Tusie-Luna MT, Lesser M, New MI, White PC. 1992J Clin Invest 90: 584-595
4. Kochhan L, Knorr D, Olek K, Bidlingmaier F. 1991 Acta Endocrinol 124 (Supp. 1):108
5. Grüters A, Morel Y. 1996 78th meeting of the Endocrine Society, San Francisco, Cal. Abstr. No. 1379