Complete androgen insensitivity syndrome, or CAIS, is a condition in which the body's cells are completely unable to respond to androgens. The insensitivity becomes clinically significant only in individuals exposed to significant amounts of testosterone at some point in their lives, since the lack of cellular response to androgenic hormones prevents the masculinization of male genitalia in the developing fetus and blocks the development of male secondary sexual characteristics at puberty, while allowing female genital and sexual development to proceed largely without impairment.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 1 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) First Described Sources
1. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVIIQuote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
View the Source 2. Wikipedia: Non-communicable disease
WikipediaLead section, transmission-route statement (inferred from disease-category)
Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
Inherited/genetic diseases section
Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
View the Source 3. Orphanet (INSERM): Orphanet: Complete androgen insensitivity syndrome (ORPHA:99429)
Orphanet (INSERM)DisorderGeneAssociationQuote, DisorderGeneAssociation
"DisorderGeneAssociationType": "Disease-causing germline mutation(s) in"
View the Source 4. Complete androgen insensitivity syndrome (Wikipedia)
History sectionQuote, History section
The first definitive description of CAIS was reported in 1817.
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