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Article

Is it time to commence newborn screening for congenital adrenal hyperplasia in Australia?

The Medical journal of Australia - 5 Sept 2011

Wu Joyce Y, Sudeep, Cowley David M, Harris Mark, McGown Ivan N, Cotterill Andrew M

Abstract excerpt

21-Hydroxylase deficiency (21-OHD) is the most common cause of congenital adrenal hyperplasia, with an incidence of 1:14000 live births and equal prevalence among males and females. Newborns with the most severe "salt-wasting" form of 21-OHD are susceptible to salt-wasting crises in the first few...

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Identifiers

PMID: 21895585
DOI: 10.5694/mja11.10284

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21895585-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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