Artigo Revisado por pares

Neonatal Screening Program for Congenital Adrenal Hyperplasia in a Homogeneous Caucasian Population

1985; Wiley; Volume: 458; Issue: 1 Linguagem: Inglês

10.1111/j.1749-6632.1985.tb14594.x

ISSN

1749-6632

Autores

E Cacciari, Antonio Balsamo, Alessandra Cassio, S. Piazzi, Filippo Bernardi, S Salardi, Alessandro Cicognani, Piero Pirazzoli, F Zappulla, Giovanni Capelli, Moreno Paolini, C. I. Cordaro,

Tópico(s)

Neonatal Health and Biochemistry

Resumo

Annals of the New York Academy of SciencesVolume 458, Issue 1 p. 85-89 Neonatal Screening Program for Congenital Adrenal Hyperplasia in a Homogeneous Caucasian Population E. CACCIARI, E. CACCIARI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorA. BALSAMO, A. BALSAMO 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorA. CASSIO, A. CASSIO 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorS. PIAZZI, S. PIAZZI 2nd Pediatric Clinic, University of Bologna Central Laboratory S. Orsola Hospital of Bologna 40138 Bologna, ItalySearch for more papers by this authorF. BERNARDI, F. BERNARDI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorS. SALARDI, S. SALARDI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorA. CICOGNANI, A. CICOGNANI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorP. PIRAZZOLI, P. PIRAZZOLI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorF. ZAPPULLA, F. ZAPPULLA 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorM. CAPELLI, M. CAPELLI 2nd Pediatric Clinic, University of Bologna Central Laboratory S. Orsola Hospital of Bologna 40138 Bologna, ItalySearch for more papers by this authorM. PAOLINI, M. PAOLINI 2nd Pediatric Clinic, University of Bologna Central Laboratory S. Orsola Hospital of Bologna 40138 Bologna, ItalySearch for more papers by this authorC.I. CORDARO, C.I. CORDARO 2nd Pediatric Clinic, University of BolognaSearch for more papers by this author E. CACCIARI, E. CACCIARI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorA. BALSAMO, A. BALSAMO 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorA. CASSIO, A. CASSIO 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorS. PIAZZI, S. PIAZZI 2nd Pediatric Clinic, University of Bologna Central Laboratory S. Orsola Hospital of Bologna 40138 Bologna, ItalySearch for more papers by this authorF. BERNARDI, F. BERNARDI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorS. SALARDI, S. SALARDI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorA. CICOGNANI, A. CICOGNANI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorP. PIRAZZOLI, P. PIRAZZOLI 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorF. ZAPPULLA, F. ZAPPULLA 2nd Pediatric Clinic, University of BolognaSearch for more papers by this authorM. CAPELLI, M. CAPELLI 2nd Pediatric Clinic, University of Bologna Central Laboratory S. Orsola Hospital of Bologna 40138 Bologna, ItalySearch for more papers by this authorM. PAOLINI, M. PAOLINI 2nd Pediatric Clinic, University of Bologna Central Laboratory S. Orsola Hospital of Bologna 40138 Bologna, ItalySearch for more papers by this authorC.I. CORDARO, C.I. CORDARO 2nd Pediatric Clinic, University of BolognaSearch for more papers by this author First published: November 1985 https://doi.org/10.1111/j.1749-6632.1985.tb14594.xCitations: 6AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Hirschfield, A. J. & J. K. Fleshman 1969. An unusually high incidence of salt-losing congenital adrenal hyperplasia in the Alaskan Eskimo. J. 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Unusual heterozygotes of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Acta Endocrinol. 87: 557–565. CASPubMedWeb of Science®Google Scholar 15 Blankstein, J., C. Faiman, F. I. Reyes, M. L. Shroeder & J. S. D. Winter 1980. Adult-onset familial adrenal 21-hydroxylase deficiency. Am. J. Med. 68: 441–448. 10.1016/0002-9343(80)90117-5 CASPubMedWeb of Science®Google Scholar 16 New, M. I., F. Lorenzen, S. Pang, P. Gunczler, B. Dupont & L. S. Levine 1979. “Acquired” adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorder as congenital adrenal hyperplasia. J. Clin. Endocrinol. Metab. 48: 356–369. 10.1210/jcem-48-2-356 CASPubMedWeb of Science®Google Scholar 17 Levine, L. S., M. Zachmann & M. I. New 1978. Genetic mapping of the 21-hydroxylase deficiency gene within the HLA linkage group. N. Eng. J. Med. 299: 911–915. 10.1056/NEJM197810262991702 CASPubMedWeb of Science®Google Scholar Citing Literature Volume458, Issue1Congenital Adrenal HyperplasiaNovember 1985Pages 85-89 ReferencesRelatedInformation

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