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Results 1 - 8 of 8 for Adrenal hyperplasia
  1. Primary macronodular adrenal hyperplasia 
    Primary macronodular adrenal hyperplasia (PMAH) is a disorder characterized by multiple lumps (nodules) in the adrenal glands, which are small hormone-producing ...
    https://medlineplus.gov/.../primary-macronodular-adrenal-hyperplasia - Genetics
  2. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency 
    Congenital adrenal hyperplasia (CAH) due to 11-beta-hydroxylase deficiency is one of a group of disorders (collectively called congenital adrenal hyperplasia) that ...
    https://medlineplus.gov/...sia-due-to-11-beta-hydroxylase-deficiency - Genetics
  3. 17 alpha-hydroxylase/17,20-lyase deficiency 
    ... 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 ...
    https://medlineplus.gov/...-alpha-hydroxylase-17-20-lyase-deficiency - Genetics
  4. Cytochrome P450 oxidoreductase deficiency 
    ... 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 ...
    https://medlineplus.gov/...cytochrome-p450-oxidoreductase-deficiency - Genetics
  5. 3-beta-hydroxysteroid dehydrogenase deficiency 
    ... of a group of disorders known as congenital adrenal hyperplasias that impair hormone production and disrupt sexual development ... deficiency 3β-HSD deficiency 3β-HSD deficiency congenital adrenal hyperplasia 3β-hydroxysteroid dehydrogenase deficiency Type II 3β-hydroxysteroid ...
    https://medlineplus.gov/...a-hydroxysteroid-dehydrogenase-deficiency - Genetics
  6. 21-hydroxylase deficiency 
    ... of a group of disorders known as congenital adrenal hyperplasias that impair hormone production and disrupt sexual development. ... about 95 percent of all cases of congenital adrenal hyperplasia. Mutations in the CYP21A2 gene cause 21-hydroxylase ...
    https://medlineplus.gov/genetics/condition/21-hydroxylase-deficiency - Genetics
  7. X-linked adrenal hypoplasia congenita 
    ... Mukai T, Nakae J. Molecular pathogenesis of lipoid adrenal hyperplasia and adrenal hypoplasia congenita. J Steroid Biochem Mol Biol. 2003 ...
    https://medlineplus.gov/.../x-linked-adrenal-hypoplasia-congenita - Genetics
  8. Bartter syndrome 
    ... signs and symptoms of the condition. Aldosteronism with hyperplasia of the adrenal cortex Bartter disease Bartter's syndrome Juxtaglomerular hyperplasia ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics