Classic Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency
Last Posted: Mar 16, 2023
- Caring for a Child with Congenital Adrenal Hyperplasia Diagnosed by Newborn Screening: Parental Health-Related Quality of Life, Coping Patterns, and Needs.
Laura Rautmann et al. International journal of environmental research and public health 2023 20(5)
- Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency - the next disease included in the neonatal screening program in Poland.
Ginalska-Malinowska Maria et al. Developmental period medicine 2018 22(2) 197-200
- CLINGEN Actionability Report for Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency - CYP21A2
ClinGen Actionability Working Group
- Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany.
Dörr Helmuth G et al. BMC endocrine disorders 2018 Jun 18(1) 37
- Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase-Deficiency: 13 Years of Neonatal Screening and Follow-up in Bavaria.
Odenwald B et al. Klin Padiatr 2015 Jun 19.
- Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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