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

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.Methods:We analyzed birth weig...

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Main Authors: Helmuth G. Dörr (Author), Theresa Penger (Author), Andrea Albrecht (Author), Michaela Marx (Author), Thomas M. K. Völkl (Author)
Format: Book
Published: Galenos Yayincilik, 2019-03-01T00:00:00Z.
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LEADER 00000 am a22000003u 4500
001 doaj_ce525c9a34cc4a34b83ba7146b3c3156
042 |a dc 
100 1 0 |a Helmuth G. Dörr  |e author 
700 1 0 |a Theresa Penger  |e author 
700 1 0 |a Andrea Albrecht  |e author 
700 1 0 |a Michaela Marx  |e author 
700 1 0 |a Thomas M. K. Völkl  |e author 
245 0 0 |a Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency 
260 |b Galenos Yayincilik,   |c 2019-03-01T00:00:00Z. 
500 |a 1308-5727 
500 |a 1308-5735 
500 |a 10.4274/jcrpe.galenos.2018.2018.0149 
520 |a 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.Methods:We analyzed birth weight and length data of 116 German newborns (48 boys, 68 girls) with classic CAH who were born during the period from 1990 to 2017. All children have been followed or are currently treated as outpatients in our clinic. All children were born at term. The mothers were healthy and their pregnancies were uneventful. The diagnosis of CAH was confirmed by molecular analyses of the CYP21A2 gene. Birth data were calculated as standard deviation (SD) scores according to German reference values.Results:Weight and length in male CAH newborns (mean ± SD) (3601±576 g; 52.4±2.85 cm) were significantly higher than in female CAH newborns (3347±442 g; 51.2±2.55 cm), but male-female differences in the CAH cohort were lost when the data were converted into SD scores. The birth sizes of the CAH newborns did not differ from the reference group. The birth sizes also did not differ between the different CAH genotypes. Maternal age, mode of delivery and maternal parity had no influence on birth size.Conclusion:Our data show that prenatal hyperandrogenism does not affect fetal growth. 
546 |a EN 
690 |a Term newborn 
690 |a congenital adrenal hyperplasia 
690 |a 21-hydroxylase deficiency 
690 |a genotype 
690 |a Pediatrics 
690 |a RJ1-570 
690 |a Diseases of the endocrine glands. Clinical endocrinology 
690 |a RC648-665 
655 7 |a article  |2 local 
786 0 |n JCRPE, Vol 11, Iss 1, Pp 41-45 (2019) 
787 0 |n  http://www.jcrpe.org/archives/archive-detail/article-preview/birth-size-in-neonates-with-congenital-adrenal-hyp/19551  
787 0 |n https://doaj.org/toc/1308-5727 
787 0 |n https://doaj.org/toc/1308-5735 
856 4 1 |u https://doaj.org/article/ce525c9a34cc4a34b83ba7146b3c3156  |z Connect to this object online.