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Hydroxylase Deficiency
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Hydroxylase Deficiency trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
See which Hydroxylase Deficiency trials may be worth asking aboutNorth America
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This study will evaluate and gather information in patients with genetic causes of too much androgen (male-like hormone) in order to better understand the effec…
This study aims to evaluate the effects of high-dose vitamin D3 supplementation on selected physiological, neuromuscular, and cognitive parameters in athletes.…
This study will attempt to identify the specific gene (coded in the DNA) and changes (mutations) within that gene that are the cause of monogenic kidney stone d…
Congenital adrenal hyperplasia (CAH) is a genetic disease with autosomal recessive transmission, which is defined by a deficiency of one of the steroidogenesis…
You are being asked to take part in this research registry because you or your family member is suspected to have a 24-hydroxylase deficiency.
Neonatal salt loss can be caused not only by infections but also by rare endocrine disorders that resemble 21-hydroxylase deficiency but are not detected by neo…
Classic congenital adrenal hyperplasia (CAH) is an autosomal recessive genetic disorder caused by a defect in the enzyme cascade regulating adrenal steroidogene…
The goal of this clinical trial is to evaluate whether a high-intensity loading dose of ergocalciferol (vitamin D2) can normalize blood vitamin D levels more ra…