Androgen insensitivity syndrome: Difference between revisions
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==[[Androgen insensitivity syndrome historical perspective|Historical Perspective]]== | ==[[Androgen insensitivity syndrome historical perspective|Historical Perspective]]== | ||
==[[Androgen insensitivity syndrome classification|Classification]]== | ==[[Androgen insensitivity syndrome classification|Classification]]== | ||
Revision as of 11:45, 13 July 2017
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Androgen insensitivity syndrome Microchapters |
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Differentiating Androgen insensitivity syndrome from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Androgen insensitivity syndrome On the Web |
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American Roentgen Ray Society Images of Androgen insensitivity syndrome |
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Directions to Hospitals Treating Androgen insensitivity syndrome |
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Risk calculators and risk factors for Androgen insensitivity syndrome |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]: Associate Editor(s)-in-Chief:
For patient information click here
Synonyms and keywords: Androgen resistance syndrome; complete androgen insensitivity; Goldberg-Morris syndrome; testicular feminization syndrome; incomplete androgen insensitivity; partial androgen insensitivity; Reifenstein syndrome; Gilbert-Dreyfus syndrome; disorder of sex development; DSD; androgen receptor; gonadal tumor; hormone replacement therapy; androgen insensitivity; androgen receptor; CAIS; complete androgen insensitivity syndrome; PAIS; partial androgen insensitivity syndrome; MAIS; mild androgen insensitivity syndrome; germ cell tumors.
| Androgen insensitivity syndrome | |
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| Testosterone (structure pictured) and dihydrotestosterone to a lesser degree, are the primary androgens involved in AIS. | |
| ICD-10 | E34.5 |
| ICD-9 | 259.5 |
| OMIM | 312300 300068 |
| DiseasesDB | 29662 Template:DiseasesDB2 |
| MeSH | D013734 |
Overview
Historical Perspective
Classification
Androgen insensitivity syndrome (AIS) represents a spectrum of defects in androgen action and can be subdivided into three broad phenotypes such as CAIS. PAIS and MAIS.
Pathophysiology
Causes
Differentiating Androgen insensitivity syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | X Ray | CT | MRI | Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
Related Chapters
- 17-hydroxylase deficiency syndrome
- 3-beta-hydroxysteroid dehydrogenase deficiency
- 5-alpha-reductase deficiency
- Congenital adrenal hyperplasia
- Mayer-rokitansky syndrome