Results 1 -
9
of
9
for
"21-hydroxylase" deficiency
- 21-hydroxylase deficiency is an inherited disorder that affects the adrenal glands. The adrenal glands are located on top of the kidneys and produce a variety ...
- Congenital adrenal hyperplasia is the name given to a group of inherited disorders of the adrenal gland . Inherited means the traits ...
- ... the CYP21A2 gene have been found to cause 21-hydroxylase deficiency. Some of these mutations result from an exchange ... to make a protein. Other mutations that cause 21-hydroxylase deficiency change single protein building blocks (amino acids) in ...
- ... 17-OHP are a sign of CAH with 21-hydroxylase deficiency. The adrenal glands use the extra 17-OHP ... usual. Classic CAH that is caused by a 21-hydroxylase deficiency can be diagnosed with 17-OHP testing. Less ...
- Adrenal Gland Disorders (National Library of Medicine)... make enough cortisol. The most common type is 21-hydroxylase deficiency (also called CAH1). In the United States, newborn ...
- Newborn Screening (National Library of Medicine)Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include: Tests ...
- Hirsutism (Endocrine Society)Excessive unwanted hair growth in women can be uncomfortable and is usually linked to an underlying endocrine disorder called hirsutism. Hirsutism is ...
- What Are the Treatments for Congenital Adrenal Hyperplasia (CAH)? (Eunice Kennedy Shriver National Institute of Child Health and Human Development)Adrenal Gland Disorders/Treatments and Therapies ... Adrenal Gland Disorders ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ...
- ... steroidogenesis Combined partial deficiency of 17-hydroxylase and 21-hydroxylase Congenital adrenal hyperplasia due to apparent combined p450c17 and p450c21 deficiency POR deficiency PORD Genetic Testing Registry: Congenital adrenal ...