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Ambiguous genitalia |
Ambiguous
genitalia
Overview
Ambiguous genitalia is a rare condition in
which an infant's external genitals don't appear to be clearly either male or
female. In a baby with ambiguous genitalia, the genitals may be incompletely
developed or the baby may have characteristics of both sexes. The external sex
organs may not match the internal sex organs or genetic sex.
Ambiguous genitalia isn't a disease, it's a
disorder of sex development. Usually, ambiguous genitalia is obvious at or
shortly after birth, and it can be very distressing for families. Your medical
team will look for the cause of ambiguous genitalia and provide information and
counseling that can help guide decisions about your baby's gender and any
necessary treatment.
Symptoms
Your medical team will likely be the first to
recognize ambiguous genitalia soon after your baby is born. Occasionally,
ambiguous genitalia may be suspected before birth (prenatally). Characteristics
can vary in severity, depending on when during genital development the problem
occurred and the cause of the disorder.
Babies who are genetically female (with two X
chromosomes) may have:
·
An enlarged clitoris,
which may resemble a penis
·
Closed labia, or labia
that include folds and resemble a scrotum
·
Lumps that feel like
testes in the fused labia
Babies who are genetically male (with one X
and one Y chromosome) may have:
·
A condition in which
the narrow tube that carries urine and semen (urethra) doesn't fully extend to
the tip of the penis (hypospadias)
·
An abnormally small
penis with the urethral opening closer to the scrotum
·
The absence of one or
both testicles in what appears to be the scrotum
·
Undescended testicles
and an empty scrotum that has the appearance of a labia with or without a
micropenis
Causes
Ambiguous genitalia primarily occurs when
hormone abnormalities during pregnancy interrupt or disturb the fetus's
developing sex organs.
How sex organs form in
the womb
A baby's genetic sex is established at
conception, based on the sex chromosomes. The mother's egg contains an X
chromosome, and the father's sperm contains either an X or a Y chromosome. A
baby who inherits the X chromosome from the father is a genetic female (two X
chromosomes). A baby who inherits the Y chromosome from the father is a genetic
male (one X and one Y chromosome).
Male and female sex organs develop from the
same tissue. Whether this tissue becomes male organs or female organs depends
on the chromosomes and the presence or absence of male hormones.
·
In males, a region on
the Y chromosome triggers the development of testicles, which produce male
hormones. Male genitals develop in response to male hormones from the fetal
testicles.
·
In a fetus without a Y
chromosome — without the effects of male hormones — the genitals develop as
female.
Occasionally, a chromosomal abnormality may
make determination of genetic sex complex.
How ambiguous
genitalia occurs
A disruption of the steps that determine sex
can result in a mismatch between the appearance of the external genitals and
the internal sex organs or the genetic sex (XX or XY).
·
A lack or deficiency
of male hormones in a genetic male fetus can cause ambiguous genitalia, while
exposure to male hormones during development results in ambiguous genitalia in
a genetic female.
·
Mutations in certain
genes can influence fetal sex development and cause ambiguous genitalia.
·
Chromosomal
abnormalities, such as a missing sex chromosome or an extra one, also can cause
ambiguous genitalia.
·
In some cases, the
cause of ambiguous genitalia may not be determined.
Possible causes in
genetic females
Causes of ambiguous genitalia in a genetic
female may include:
·
Congenital
adrenal hyperplasia. Certain forms of
this genetic condition cause the adrenal glands to make excess male hormones
(androgens).
·
Prenatal
exposure to male hormones. Certain
drugs that contain male hormones or that stimulate production of male hormones
in a pregnant woman can cause developing female genitals to become more
masculine. A developing baby also may be exposed to excess male hormones if the
mother has a disease or condition that causes hormone imbalance.
·
Tumors. Rarely, a tumor in the mother can
produce male hormones.
Possible causes in
genetic males
Causes of ambiguous genitalia in a genetic
male may include:
·
Impaired
testicle development. This may be due
to genetic abnormalities or unknown causes.
·
Androgen
insensitivity syndrome. In
this condition, developing genital tissues don't respond normally to male
hormones made by the testes.
·
Abnormalities
with testes or testosterone. Various abnormalities can interfere with the testes'
activity. This may include structural problems with the testes, problems with
production of the male hormone testosterone or problems with cellular receptors
that respond to testosterone.
·
5a-reductase
deficiency. This enzyme
defect impairs normal male hormone production.
Ambiguous genitalia can also be a feature of
certain rare, complex syndromes that affect many organ systems.
Risk factors
Family history may play a role in the
development of ambiguous genitalia, because many disorders of sex development
result from genetic abnormalities that can be inherited. Possible risk factors
for ambiguous genitalia include a family history of:
·
Unexplained deaths in
early infancy
·
Infertility, absent
menstrual periods or excess facial hair in females
·
Genital abnormalities
·
Abnormal physical
development during puberty
·
Congenital adrenal
hyperplasia, a group of inherited genetic disorders that affect the adrenal
glands
If your family has a history of these risk
factors, consider seeking medical advice before trying to conceive. You may
also benefit from genetic counseling.
Complications
Complications of ambiguous genitalia may
include:
·
Infertility. Whether people with ambiguous genitalia
can have children depends on the specific diagnosis. For example, genetic
females with congenital adrenal hyperplasia usually can get pregnant if they so
choose.
·
Increased
risk of certain cancers. Some
disorders of sex development are associated with an increased risk of certain
types of cancer.
Diagnosis
Ambiguous genitalia is usually diagnosed at
birth or shortly after. Doctors and nurses who help with delivery may notice
the signs of ambiguous genitalia in your newborn.
Determining the cause
If your baby is born with ambiguous genitalia,
the doctors will work to determine the underlying cause. The cause helps guide
treatment and decisions about your baby's gender. Your doctor will likely begin
by asking questions about your family and medical history. He or she will do a
physical exam to check for testes and evaluate your baby's genitalia.
Your medical team will likely recommend these
tests:
·
Blood tests to measure
hormone levels
·
Blood tests to analyze
chromosomes and determine the genetic sex (XX or XY) or tests for single gene
disorders
·
Ultrasound of the pelvis
and abdomen to check for undescended testes, uterus or vagina
·
X-ray studies using a
contrast dye to help clarify anatomy
In certain cases, minimally invasive surgery
may be necessary to collect a tissue sample of your newborn's reproductive
organs.
Determining the gender
Using the information gathered from these
tests, your doctor may suggest a gender for your baby. The suggestion will be
based on the cause, genetic sex, anatomy, future reproductive and sexual
potential, probable adult gender identity, and discussion with you.
In some cases, a family may make a decision
within a few days after the birth. However, it's important that the family wait
until test results are completed. Sometimes gender assignment can be complex
and the long-term impact can be difficult to predict. Parents should be aware
that as the child grows up, he or she may make a different decision about
gender identification.
Treatment
Once you and your doctor have chosen a gender
for your baby, you may choose to begin treatment for ambiguous genitalia. The
goal of treatment is long-term psychological and social well-being, as well as
to enable sexual function and fertility to the greatest extent possible. When
to begin treatment depends on your child's specific situation.
Ambiguous genitalia is uncommon and complex,
and it may require a team of experts. The team might include a pediatrician,
neonatologist, pediatric urologist, pediatric general surgeon, endocrinologist,
geneticist, and psychologist or social worker.
Medications
Hormone medications may help correct or
compensate for the hormonal imbalance. For example, in a genetic female with a
slightly enlarged clitoris caused by a minor to moderate case of congenital
adrenal hyperplasia, proper levels of hormones may reduce the size of the
tissue. Other children may take hormones around the time they would normally
experience puberty.
Surgery
In children with ambiguous genitalia, surgery
may be used to:
·
Preserve normal sexual
function
·
Create genitals that
appear more typical
The timing of surgery will depend on your
child's specific situation. Some doctors prefer to postpone surgery done solely
for cosmetic reasons until the person with ambiguous genitalia is mature enough
to participate in the decision about gender assignment.
For girls with ambiguous genitalia, the sex
organs may work normally despite the ambiguous outward appearance. If a girl's
vagina is hidden under her skin, surgery in childhood can help with sexual
function later. For boys, surgery to reconstruct an incomplete penis may
normalize appearance and make erections possible. Surgery to reposition the
testes into the scrotum may be required.
Results of surgery are often satisfying, but
repeat surgeries may be needed later. Risks include a disappointing cosmetic
result or sexual dysfunction, such as an impaired ability to achieve orgasm.
Ongoing care
Children with ambiguous genitalia require
ongoing medical care and monitoring for complications, such as cancer
screenings, into adulthood.
Coping and support
If your baby is diagnosed with ambiguous
genitalia, you may worry about your child's future. Mental health professionals
can help you deal with this difficult and unexpected challenge. Ask your
child's doctor for a referral to a mental health professional who has experience
helping people in your situation.
In addition to ongoing counseling for your
family and your child, you may benefit from a support group, either in person
or online. Your child can benefit from ongoing counseling by mental health
professionals and participation in support groups into adulthood.
Not knowing the gender of your newborn
immediately can turn a hoped-for celebration into a stressful crisis. Your
medical team will provide you with updates and information as quickly as
possible to help settle any questions about your child's health.
Consider delaying a formal announcement of the
birth until testing is complete and you've developed a plan with advice from
your medical team. Give yourself some time to learn and think about the issue
before answering difficult questions from family and friends.
Preparing for your
appointment
If your baby was born with ambiguous
genitalia, you may be referred to a medical center with doctors who have
expertise in this condition. Here's some information to help you get ready for
your appointment and learn what to expect from your doctor.
What you can do
Before your appointment:
·
Ask
if there's anything you need to do in advance to prepare your infant for tests and procedures.
·
Discuss
family history with your relatives and bring key personal information, including family history of genetic
diseases or conditions, such as ambiguous genitalia.
·
Consider
taking a family member or friend along. Sometimes it can be difficult to remember all the
information provided during an appointment. Someone who accompanies you may
remember something that you missed or forgot.
·
Make
a list of questions to ask your
doctor.
Questions to ask your doctor may include:
·
What caused my baby's
uncertain genitalia?
·
What genetic testing
has been completed?
·
What other tests might
my baby need?
·
What is the best
course of action?
·
What are the
alternatives to the primary approach that you're suggesting?
·
Is there a generic
alternative to the medicine you're prescribing?
·
Are there any
restrictions that my baby needs to follow?
·
Should my baby see any
other specialists?
·
What options are there
for counseling and support for our family?
·
Are there brochures or
other printed materials that I can have? What websites do you recommend?
Don't hesitate to ask other questions during
your appointment.
What to expect from
your doctor
Your doctor is likely to ask you several
questions, such as:
·
Does your family have
a history of ambiguous genitalia?
·
Does your family have
a history of other genetic diseases?
·
Do any diseases or
conditions tend to run in your family?
·
Have you ever had a
miscarriage?
·
Have you ever had a
child who died in infancy?
Be ready to answer questions to allow more
time to cover other points you want to address.
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