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Results 1 - 10 of 18 for 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 
    ... a group of disorders, known as congenital adrenal hyperplasias, that impair hormone production and disrupt sexual development ... 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 
    ... 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. Rabson-Mendenhall syndrome 
    ... and symptoms of the condition. Mendenhall syndrome Pineal hyperplasia and diabetes mellitus syndrome Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities RMS ...
    https://medlineplus.gov/.../condition/rabson-mendenhall-syndrome - Genetics
  6. Bartter syndrome 
    ... signs and symptoms of the condition. Aldosteronism with hyperplasia of the adrenal cortex Bartter disease Bartter's syndrome Juxtaglomerular hyperplasia with secondary aldosteronism Genetic Testing Registry: Antenatal Bartter ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  7. 3-beta-hydroxysteroid dehydrogenase deficiency 
    ... a group of disorders known as congenital adrenal hyperplasias that impair hormone production and disrupt sexual development ... 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
  8. Frontonasal dysplasia 
    Frontonasal dysplasia is a condition that results from abnormal development of the head and face before birth. People with frontonasal dysplasia have at least two ...
    https://medlineplus.gov/genetics/condition/frontonasal-dysplasia - Genetics
  9. Cowden syndrome 
    Cowden syndrome is a genetic disorder characterized by multiple noncancerous, tumor-like growths called hamartomas and an increased risk of developing certain ...
    https://medlineplus.gov/genetics/condition/cowden-syndrome - Genetics
  10. 21-hydroxylase deficiency 
    ... a group of disorders known as congenital adrenal hyperplasias that impair hormone production and disrupt sexual development. ... 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
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