How would I go about getting a genetic test for polycystic kidney disease before ttc?

Genetic Counselor. See a genetic counselor to arrange testing. University hospitals have clinical or medical genetics divisions. Otherwise, your OB doctor, a fertility clinic, or a maternal fetal medicine or high-risk OB clinic can refer you. If the testing is positive, see a reproductive endocrinologist before you get pregnant to discuss preimplantation genetic diagnosis (pgd) to prevent your child from having pckd.

Related Questions

How would I go about getting a genetic test for polycystic kidney disease (pkd) to see if I might pass it on?

See your doctor. The best place to start is with your primary care physician. A very thorough family history and an ultrasound will help determine if you have pkd. You will need to see a nephrologist and maybe a geneticist to determine what kind of PKD you have. The risk of passing PKD to your children depends on getting the correct diagnosis. Genetic testing would usually be ordered by one of those specialists. Read more...

How do I find out if I have pkd (polycystic kidney disease) without having expensive genetic testing?

Ultrasound. You can take an imaging study called a renal ultrasound. The ultrasound can determine the number of cysts on your kidneys and can lead to a diagnose of polycystic kidney disease. Read more...
PKD testing. The gold standard after age 30 is ultrasound of the kidneys. This is not expensive and if you have no cysts at your age, then you do not have PKD. Genetic testing is not the standard. Read more...

What to do if I have 4-month old girl patient with polycystic kidney disease. W/o genetic studies, how do I know w/c type?

Polycystic kidneys. You have a wonderful children's hospital in Philadelphia. Call their urology department for help with your infant daughter.Their genetics department will also bevery helpful. Read more...
3 main possibilities. Infantile polycystic kidney disease, an autosomal recessive, causes huge kidneys with a homogenous appearance on ultrasound. A non-genetic condition, multicystic kidney, may be uni- or bilateral, and have discreet round cysts--sonolucencies of varying sizes, sometimes in a single pole. Adult polycystic kidney disease may rarely appear in infancy, and is an autosomal dominant, affecting both. Read more...

How do you test for polycystic kidney disease?

Renal Ultrasound. Polycystic kidney disease is usually diagnosed by taking a renal ultrasound of your kidneys to determine the number of cysts that are on each kidney. Usually, a person presnts with bloody urine or multiple UTI that will lead to a doctor taking a patient of the kidneys and diagnosing the issue. Read more...
Imaging. With ultrasound is usually how the disease gets diagnosed. There are genetic tests available now as well for patients with family histories. Read more...
PKD Diagnosis. PKD is diagnosed by renal ultrasound. BY age 30, an affected person will have 3 or more cysts per kidney. Family history is relevant also. Renal MRI is more accurate but more expensive. Genetic testing can be very precise but is expensive. Read more...

Is it dangerous to get pregnant and have a baby if you have polycystic kidney disease?

No but......... Pregnancy is successful for most women with polycystic kidney disease. However, they may develop a life-threatening disorder called preeclampsia. Those most at risk are women who have high blood pressure before they become pregnant. Read more...

What type of haematology tests are involved in polycystic kidney disease?

Routine. Pckd is a genetic disorder that results in architectural cysts within the kidney. Routine labs to look at hemoglobin level, basic chemistries and urinalysis are preformed. An ultrasound or ct scan can help with characterizing cysts. Read more...