Examining Genetic Differences Among People With 21-Hydroxylase Deficiency

Completed · Not applicable

Conditions studied: 21-hydroxylase Deficiency

In brief

Congenital adrenal hyperplasia (CAH) is a genetic disorder that affects the amount of steroids that the body forms. The most common form of CAH is 21-hydroxylase deficiency (21OHD), which leads to cortisol deficiency. This, in turn, causes the development of mature masculine characteristics in newborn, prepubescent, and grown females and in prepubescent males. 21OHD is known to be caused by the mutation of a specific gene. However, symptom severity among people with 21OHD varies, and adults seem to be less affected than children. This study will examine participants' DNA to determine what other genes may affect the severity of 21OHD and may make the disease milder in adults than in children.

Key facts

Study ID
NCT00542841
Run by
Maria I. New
People needed
99
Starts
2007-08-01
Expected to finish
2009-03-01
Last updated by the study team
2015-12-14

Who can join

Age: 18 and older, up to 50. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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