Sy Borg wrote: ↑April 1st, 2024, 2:30 pm
Consul wrote: ↑April 1st, 2024, 1:57 pm[Note that most of the 0.02% of "intersexuals" (= people afflicted with some disorder of sex development or other) are classifiable as either female or male!]
I have highlighted the key word in the above.
I cannot see why you think any of this is your business, or how you can make assumptions about people you know nothing about.
Oh dear! I know you're an intelligent person, so this reply of yours is very disappointing.
I've read scientific books & papers about intersexuals, so I do know something about them (although I'm far from being an expert).
Most intersexuals are classifiable as either female or male,
because they have undergone gonadal differentiation into ovaries or testicles.
An intersexual individual is
not classifiable as either female or male if and only if (1) gonadal differentiation didn't occur at all (
complete gonadal dysgenesis), or (2) gonadal differentiation did occur but resulted in both types of gonads (
true hermaphroditism).
* The overall percentage of intersexual babies born with some disorder of sex development or other is
~0.02%.
* The percentage of intersexual babies born with
complete gonadal dysgenesis is
~0.0007% (1:150000 births—see below!). So the number of intersexual babies
with CGD is
~28 times lower than the number of intersexual babies.
*
95% of all human intersexuals are
not true hermaphrodites (see below!).
Therefore, my statement that
most intersexuals are classifiable as either female or male is fully warranted by the empirical data!
"True hermaphrodite is one of the rarest variety of disorders of sexual differentiation (DSD) and represents only 5% cases of all.
…
In this condition gonads are asymmetrical having both ovarian and testicular differentiation on either sides separately or combined as ovotestis."
Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418019/
"Complete Gonadal Dysgenesis:
The Complete form of Gonadal Dysgenesis is proposed as occurring once in every 150,000 births (Blackless et al. 2000). It affects genetic males (46,XY karyotype) and genetic females (46,XX karyotype), as well as individuals with the 45,XO karyotype (…). In Complete Gonadal Dysgenesis, the typical differentiation of the gonads as either testes or ovaries does not occur. They form atypically as underdeveloped and undescended streak gonads, and there is complete absence of ovaries, testes or ovotestes. Streak gonads differ from ovotestes (which contain both ovarian and testicular tissue) being undeveloped whorled gonadal structures without germinal or secretory cells. They fail to produce the androgens necessary for masculine differentiation of the genitalia, and consequently female-appearing external genitalia form. Streak gonads are also incapable of ovulation or oestrogen secretion. Clitoral hypertrophy (enlargement), and sexual infantilism (delayed or absent puberty) may also be experienced (Jha undated)."
(Harper, Catherine. Intersex. Oxford: Berg, 2007. p. 129)