Androgen insensitivity syndrome: Difference between revisions

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==[[Androgen insensitivity syndrome historical perspective|Historical Perspective]]==
==[[Androgen insensitivity syndrome historical perspective|Historical Perspective]]==
Case reports compatible with CAIS date back to the 19th century, when hermaphroditism was the technical term for intersex conditions.


==[[Androgen insensitivity syndrome classification|Classification]]==
==[[Androgen insensitivity syndrome classification|Classification]]==

Revision as of 11:44, 13 July 2017

Androgen insensitivity syndrome Microchapters

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Overview

Historical Perspective

Classification

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

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Treatment

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Cost-Effectiveness of Therapy

Future or Investigational Therapies

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Case #1

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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
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

Case reports compatible with CAIS date back to the 19th century, when hermaphroditism was the technical term for intersex conditions.

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

Case #1

Related Chapters

References

androgen at NIH/UW GeneTests

de:Komplette Androgenresistenz it:Sindrome di Morris


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