adrenal hyperplasia


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adrenal hyperplasia

Diffuse enlargement of the adrenal glands. See Congenital adrenal hyperplasia.
References in periodicals archive ?
Congenital adrenal hyperplasia (CAH) caused by deficiency of the 21-hydroxylase enzyme is the most common form of CAH worldwide.
Congenital adrenal hyperplasia secondary to 3-beta hydroxysteroid dehydrogenase deficiency
CARES Foundation, an organization that leads the effort to improve the lives of the congenital adrenal hyperplasia community, wholeheartedly supports a thorough discussion of CAH.
Congenital adrenal Hyperplasia due to 21-hydroxylase deficiency presenting as adrenal incidentaloma: a systematic review and meta-analysis.
Congenital Adrenal Hyperplasia (CAH) is an orphan condition usually caused by deficiencyof the enzyme 21- hydroxylase.
Adrenal steroidogenesis and congenital adrenal hyperplasia.
Seventeen alpha-hydroxylase deficiency is a rare form of congenital adrenal hyperplasia (CAH), with about 150 cases reported in the world literature.
Divergent gender identity in three siblings with 46 XX karyotype and severely virilising congenital adrenal hyperplasia caused by a novel CY11B1 mutation.
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X
Congenital adrenal hyperplasia (CAH) is caused by defects in one of the steroidogenic enzymes involved in the adrenal steroid biosynthesis from cholesterol to cortisol.
Medical management is the treatment of choice in bilateral adrenal hyperplasia, or when surgery cannot be performed.
GlobalData's clinical trial report, "Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) Global Clinical Trials Review, H2, 2015" provides an overview of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome) clinical trials scenario.

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