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Adrenal hyperplasia
- Primary macronodular adrenal hyperplasia (PMAH) is a disorder characterized by multiple lumps (nodules) in the adrenal glands, which are small hormone-producing ...
- Congenital adrenal hyperplasia (CAH) due to 11-beta-hydroxylase deficiency is one of a group of disorders (collectively called congenital adrenal hyperplasia) that ...
- Adrenal Gland Disorders (National Library of Medicine)... cancerous tumors, including adrenocortical carcinoma and neuroblastoma Congenital Adrenal Hyperplasia (CAH) - a group of inherited disorders in which ...
- Congenital Adrenal Hyperplasia (For Parents) (Nemours Foundation)Adrenal Gland Disorders/Children ... Adrenal Gland Disorders ... Nemours Foundation ... Congenital Adrenal Hyperplasia, hyperplasia, adrenal, adrenal glands, glands, ...
- Congenital adrenal hyperplasia is the name given to a group of inherited disorders of the adrenal gland . Inherited means the ... both males and females. Most people with congenital adrenal hyperplasia (CAH) lack an enzyme called 21-hydroxylase. The ...
- ... of a group of disorders, known as congenital adrenal hyperplasias, that impair hormone production and disrupt sexual development ... deficiency accounts for about 1 percent of congenital adrenal hyperplasia cases. It is estimated to occur in 1 ...
- Congenital Adrenal Hyperplasia (CAH)
(Eunice Kennedy Shriver National Institute of Child Health and Human Development)
Congenital adrenal hyperplasia (CAH), refers to a group of genetic disorders that affect the adrenal glands, which sit atop the ... - 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 ... - ... cytochrome P450, subfamily XXIA (steroid 21-hydroxylase, congenital adrenal hyperplasia), polypeptide 2 Cytosteroid 21-Monooxygenase P450c21B steroid 21- ...
- ... 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 hyperplasia due to cytochrome P450 oxidoreductase deficiency Antley-Bixler ...