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Culture Documents
Psychosomatic
Medicine
Diamond's excellent
papers
have
genitalia
received little notice
from clinicians
and have come to my attention only after the
completion of this study.
Variables Possibly Determining Gender Role
in Parallel Order
G
E
N
D
E
R
R
0
L
The question arises whether such a method
of dealing with the data is any more justified
451
ZUGER
A change or failure of
any one variable in the
series alters the whole
series. What is finally
evident is the result of
the
sequential
influences or lack of
influences
(as,
for
instance, in the failure
of
the
embryonic
gonadal male hormone
in the Jost syndrome)
of a number of factors.
The
result
may
become
evident
at
birth,
as
in
the
adrenogenital
syndrome, or not until
puberty,
when
the
whole series is called
into action, as in other
types of pseudoherma
phrodi tism.
Furthermore,
the
basis for snaking the
sex
assignment
in
these uncertain cases
before they reached the
notice of the inves-
tigators
must
have
been the appearance
of
the
external
genitalia. It would be
just as valid, therefore,
to say that gender role
was determined by the
appearance
of
the
external genitalia at
birth as by the sex
assignment
and
rearing. Cappon (17)
makes a similar point.
This is well illustrated
in the case of the
adrenogenital
syndrome.
Money
and
the
Hampsons
presented
42 patients with this
syndrome, 38 of whom
were
assigned
the
female role and 4, the
male role. Except for 1
patient assigned the
female
role
who
subsequently
was
bisexual,
they
all
stayed with their sex
assignment. But why
were the 4 patients
assigned
the
male
role?
Was
it
the
increased, and perhaps
earlier,
virilization,
evident in the external
genitalia, which led to
their male assignment?
The extent of fusion of
the labioscrotal folds
varies in different individuals
with
this
syndrome; in some, it
may
traverse
the
enlarged clitoris in its
entirety (14). The 2
groups given gender
roles according to their
external genitalia may
not,
therefore,
be
comparable
in
evaluating sex rearing.
Another methodologic
diffi culty in the paper
of
Money
and
the
Hampsons is that they
do
not
exclude
alternative possibilities
in
comparing
separately
each
variable
with
the
gender
role
assignment. To show,
for instance, that male
sex
assignment
is
dominant over female
"endogenous hormonal
sex" in a cryptorchid
male
hypospadiac
patient
with
breasts
(male pseudohermaphrodite) (Table 4) (11),
all the other variables
would have to be
female. That is not
the
case
in
this
example, nor is it
correspondingly so in
any of their other
comparisons.
In addition to these
objections, there were
factors
to
which
Money
and
the
Hampsons could not
give adequate consideration because these
factors
were
not
known at the time they
wrote their principal
papers.
These
are
452
schematically
rep-
followedie, according
to
the
individual
variables considered.
1.
Chromosomes
and
rearing
contradictory
(Table
1).* This group consists of 19 of the 76
cases with "somatic
ambisexual
development"
which
the authors give as
evidence
of
the
overriding influence of
rearing, compared with
the
influence
of
chromosomes
in
determining gen*Table 2 in the paper
by Money et al.
GONADAL
---*HYPOTHALAMUS
Possible early1 ' Releasing
sexualization
f ,fa ctors
I --ANTERIOR
I
+ PITUITARY
I
HORMONAL
ADRENAL
Chromosomalmosaics
INTERNAL
GENITALIA
difficult
to
exclude;
EXTERNAL
GENITALIA
multiple tissues must
I
be examined.
SECONDARY SEX
CHARACTERISTIC
Gonadalunless
S
embryonic male hormone present, tendency for
develop. ment to proceed in female direction;
existence of a critical period for sexualization
of brain? Testes may secrete estrogens.
HormonalTestosterone levels may vary with
chromosomal constitution eg, extra X in
phenotypic males with low testosterone output.
Genitaliainsensitivity
of
cells
to
corresponding
hormoneseg,
testicular
feminizing syndrome.
Secondary
sex
characteristicsmay
at
puberty be opposite to earlier manifestations.
SEX ASSIGNMENT
and REARING
GENDER ROLE
ZUGER
Table 1. Chromosomes and Rearing
Contradictory (19 Cases)*
Ass
Type of Chr
Ge No
ign
ambisexu
n
.
Gonadal om
M
F
F 11
agenesis
(dysgenes
Simulant
M
F
F
3
female
Cryptor
chid
True
hermaphr
Comment
Probably cases of Turner's syndrome
and of XO karyotypes (though may be
mosaics and of other karyotypes);
called males here because of absence
of nuclear chromatin; no contradiction
between chromosomes and gender
role
More recently called cases of testicular
feminizing syndrome; no failure in
testosterone production except in its
utilization by the target organs; chromosomes not a relevant issue
Three of these are called juveniles;
their subsequent acceptance of assigned gender role unpredictable
Gonads, hormones, internal and external genitalia indicated to be both
male and female
M, male; F, female.
* Table 2 in the paper by Money et al.
f Sex chromosome type inferred from
nuclear chromatin of biopsied skin.