This is the case for instance in androgen insensitivity syndrome.

Men with mild androgen insensitivity syndrome may have reduced fertility.

A number of famous models and actresses are thought to have androgen insensitivity syndrome.

Male gender identities among a minority of individuals with complete androgen insensitivity syndrome, have also been reported.

Some men can have a hormone or chromosomal difference (for example "androgen insensitivity syndrome").

Alternatively, it may be the result of conditions such as androgen insensitivity syndrome or hyperestrogenism.

Complete androgen insensitivity syndrome: Long-term medical, surgical and psychosexual outcome.

The main causes are Müllerian agenesis and complete androgen insensitivity syndrome.

Mild androgen insensitivity syndrome generally causes no developmental issues and people with this form are raised as males.

It is considered a form of androgen insensitivity syndrome and is the most severe form.

As with other intersex conditions, androgen insensitivity syndrome is independent of both sexual orientation and gender identity.

Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UK.

Individuals with complete androgen insensitivity syndrome are almost always brought up as females, and the differentiation of gender identity/role is feminine.

A reason for this occurrence may be that a person phenotypically female but genetically male, a situation known as androgen insensitivity syndrome.

An affected 46,XY child will have androgen insensitivity syndrome.

For related phenomena, see Androgen insensitivity syndrome and Intersex.

Some of these gene or chromosome abnormalities cause intersexed conditions, such as androgen insensitivity syndrome.

His experiment is the first documented demonstration of the pathophysiology of androgen insensitivity syndrome.

A man with androgen insensitivity syndrome produces androgens and testosterone but their body does not recognize it, either partially or completely.

Estimates for the incidence of androgen insensitivity syndrome are based on a relatively small population size, and thus are known to be imprecise.

MAIS is the mildest and least known form of androgen insensitivity syndrome.

Because they do not have ovaries or sufficiently developed testicles, people with complete androgen insensitivity syndrome are infertile.

While men generally do not need any specialized medical care related to this form, mild androgen insensitivity syndrome may result in gynecomastia and hypospadias.

Androgen insensitivity syndrome is the largest single entity that leads to 46,XY undermasculinization.

Some have speculated that Semenya's particular condition is something called partial androgen insensitivity syndrome, which occurs in one of every 130,000 births.