Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia

Sze May Ng; Karolina Stepien

doi:10.1002/14651858.CD012517

Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia

Sze May Ng^*
, Karolina Stepien

^*Corresponding author for this work

Medical School

Research output: Contribution to journal › Article (journal) › peer-review

12 Citations (Scopus)

Abstract

This is a protocol for a Cochrane Review (Intervention). The objectives are as follows: To compare and determine the efficacy and safety of different glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency CAH in children and adults.

Original language	English
Article number	CD012517
Journal	Cochrane Database of Systematic Reviews
Volume	2017
Issue number	1
DOIs	https://doi.org/10.1002/14651858.CD012517
Publication status	Published - 18 Jan 2017

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10.1002/14651858.CD012517

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title = "Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia",

abstract = "This is a protocol for a Cochrane Review (Intervention). The objectives are as follows: To compare and determine the efficacy and safety of different glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency CAH in children and adults.",

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N2 - This is a protocol for a Cochrane Review (Intervention). The objectives are as follows: To compare and determine the efficacy and safety of different glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency CAH in children and adults.

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Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia

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