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Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency

Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency: Introduction

Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency: A rare form of congenital adrenal hyperplasia characterized by a deficiency of 11-Beta-hydroxylase which results in excess androgen production and hypertension. The disorder can occur in virilizing, hypertensive and salt-wasting forms and symptoms may range from mild to severe. More detailed information about the symptoms, causes, and treatments of Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency is available below.

Symptoms of Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency

  • Ambiguous external female genitalia
  • Hypertension
  • Masculinization of female infants
  • Precocious male puberty
  • Premature skeletal maturation
  • more symptoms...»

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Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency: Complications

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Causes of Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency

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Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency: Undiagnosed Conditions

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Definitions of Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency:

Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency, or a subtype of Adrenal hyperplasia, congenital, due to 11-Beta-hydroxylase deficiency, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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