Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency

Dörr HG, Penger T, Albrecht A, Marx M, Völkl T (2019)

Publication Type: Journal article

Publication year: 2019

Journal

JCRPE Journal of Clinical Research in Pediatric Endocrinology Pubbiz Publishing Solutions

Book Volume: 11

Pages Range: 41-45

Journal Issue: 1

DOI: 10.4274/jcrpe.galenos.2018.2018.0149

Abstract

Objective: Classic congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency is characterized by increased prenatal adrenal androgen secretion. There are a small number of reports in the literature showing higher birth weight and length in CAH newborns.

Authors with CRIS profile

Helmuth-Günther Dörr Professur für Kinderheilkunde mit dem Schwerpunkt Kinder-Endokrinologie und Diabetologie (Stiftungsprofessur) Theresa Penger Professur für Kinderheilkunde mit dem Schwerpunkt Kinder-Endokrinologie und Diabetologie (Stiftungsprofessur) Andrea Albrecht Lehrstuhl für Kinder- und Jugendmedizin Thomas Völkl Medizinische Fakultät

How to cite

APA:

Dörr, H.-G., Penger, T., Albrecht, A., Marx, M., & Völkl, T. (2019). Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency. JCRPE Journal of Clinical Research in Pediatric Endocrinology, 11(1), 41-45. https://doi.org/10.4274/jcrpe.galenos.2018.2018.0149

MLA:

Dörr, Helmuth-Günther, et al. "Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency." JCRPE Journal of Clinical Research in Pediatric Endocrinology 11.1 (2019): 41-45.

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