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Polycystic Kidney Disease
Polycystic Kidney Disease
WHO IS AT RISK?
Anyone with a family history of the condition.
The autosomal dominant form of the disease,
known as autosomal dominant polycystic disease,
ADPKD is the most common form.
Because this condition usually goes undiagnosed
till a person is about 30 years, many people go
through their early adulthood without knowledge
of this condition.
A history of a family member with kidney
problems should raise suspicion as early diagnosis
results in better management.
There is a 50-50 chance that you or your siblings
will get this condition from an affected parent.
There is also a 50-50 chance that you will pass this
on to your children.
Most people go for genetic counselling when
diagnosed with PKD and often consider other
available options to become a parent if they want
to break the inheritance pattern.
It occurs equally in males and females.
HOW IS IT DIAGNOSED?
In a number of cases, it is found as an incidental
finding during ultrasound of your tummy.
A family history of PKD may be the reason to
undergo a screening .
Ultrasound of the kidneys shows the cysts and the
size of the kidneys.
However, sometimes, these cysts may be too
small at the time of the scan to be seen.
Genetic testing may also be done to determine if
a faulty gene was inherited from your family.
Ultrasound of your liver is often also done as
these cysts may be present in your liver too. This
often does not cause problems unless they
become infected.
Other tests like a special scan of your brain known
as an MRI may be done to rule out enlarged blood
vessels known as aneurysms which also may be
found in people with PKD.