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Male pseudohermaphroditism, incomplete hereditary (type 1)

Male pseudohermaphroditism, incomplete hereditary (type 1): Introduction

Male pseudohermaphroditism, incomplete hereditary (type 1): A rare condition involving a deficiency of dihydrotestosterone receptor which impairs the function of androgen receptors and hence the androgen (male hormone) is partially or completely ineffective depending on the level of deficiency. The degree of feminization ranges from feminine phenotype through to male phenotype depending on the level of androgen insensitivity. More detailed information about the symptoms, causes, and treatments of Male pseudohermaphroditism, incomplete hereditary (type 1) is available below.

Symptoms of Male pseudohermaphroditism, incomplete hereditary (type 1)

  • Phenotypic female
  • Pseudovagina
  • Sterile male
  • Scanty body hair
  • Testes in abdomen
  • more symptoms...»

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Male pseudohermaphroditism, incomplete hereditary (type 1): Related Patient Stories

Male pseudohermaphroditism, incomplete hereditary (type 1): Complications

Read more about complications of Male pseudohermaphroditism, incomplete hereditary (type 1).

Causes of Male pseudohermaphroditism, incomplete hereditary (type 1)

Read more about causes of Male pseudohermaphroditism, incomplete hereditary (type 1).

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More information about Male pseudohermaphroditism, incomplete hereditary (type 1)

  1. Male pseudohermaphroditism, incomplete hereditary (type 1): Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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