1. Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
- Author
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Völkl Tmk, Helmuth G. Dörr, Theresa Penger, Michaela Marx, and Andrea Albrecht
- Subjects
Male ,medicine.medical_specialty ,congenital, hereditary, and neonatal diseases and abnormalities ,endocrine system diseases ,Endocrinology, Diabetes and Metabolism ,Birth weight ,genotype ,Term newborn ,21-hydroxylase deficiency ,urologic and male genital diseases ,lcsh:Diseases of the endocrine glands. Clinical endocrinology ,Cohort Studies ,Endocrinology ,Congenital adrenal hyperplasia due to 21-hydroxylase deficiency ,Germany ,Medicine ,Birth Weight ,Humans ,congenital adrenal hyperplasia ,Congenital adrenal hyperplasia ,lcsh:RC648-665 ,Adrenal Hyperplasia, Congenital ,business.industry ,Obstetrics ,Hyperandrogenism ,Infant, Newborn ,lcsh:RJ1-570 ,nutritional and metabolic diseases ,lcsh:Pediatrics ,medicine.disease ,Birth size ,Body Height ,female genital diseases and pregnancy complications ,Androgen secretion ,Pediatrics, Perinatology and Child Health ,Cohort ,Classic Congenital Adrenal Hyperplasia ,Original Article ,Female ,business - 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. 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.
- Published
- 2019