Results 1 - 9 of 9 for "21-hydroxylase" deficiency
  1. Genetics Home Reference: 21-hydroxylase deficiency From the National Institutes of Health (National Library of Medicine)  
    ... PubMed Recent literature OMIM Genetic disorder catalog Conditions > 21-hydroxylase deficiency On this page: Description Genetic changes Inheritance Diagnosis ...
  2. Adrenogenital syndrome; 21-hydroxylase deficiency
  3. 17-Hydroxyprogesterone Test (American Association for Clinical Chemistry)  
    ... to detect congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. CAH is a group of inherited disorders caused ... onset" form. Monitoring If someone is diagnosed with 21-hydroxylase deficiency, a 17-OHP test may be used periodically ...
  4. 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 ...
  5. Congenital Adrenal Hyperplasia From the National Institutes of Health (National Institute of Child Health and Human Development)  
    ... virilism Congenital adrenal hyperplasia (classic or nonclassic) CAH 21-hydroxylase deficiency Last Updated Date: 07/31/2013 Last Reviewed ...
  6. What Are the Treatments for Congenital Adrenal Hyperplasia (CAH)? From the National Institutes of Health (National Institute of Child Health and Human Development)  
    ... Society. (2010). Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: An Endocrine Society clinical practice guideline. Journal of ...
  7. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... Steroid Disorders Consortium (RGSDC) Disorders of Androgen Excess: 21-Hydroxylase deficiency 11b-Hydroxylase deficiency Disorders of Androgen Synthesis or ...
  8. Adrenal Gland Disorders (National Library of Medicine)  
    The adrenal glands are small glands located on top of each kidney. They produce hormones that you can't live without, including sex hormones and cortisol. ...
  9. ... steroidogenesis combined partial deficiency of 17-hydroxylase and 21-hydroxylase congenital adrenal hyperplasia due to apparent combined p450c17 and p450c21 deficiency PORD POR deficiency For more information about naming ...
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