What is the chance of having three babies with potters syndrome?

Potter's syndrome refers to a rare kidney condition that occurs in utero and is characterized by the absence or severe underdevelopment of the kidneys, leading to a lack of amniotic fluid. The exact chance of having three babies with Potter's syndrome is difficult to determine as it depends on various factors, including the underlying cause and genetics.

Potter's syndrome can occur due to a combination of genetic factors, environmental influences, and maternal conditions during pregnancy. In some cases, it may result from a specific genetic mutation or chromosomal abnormality, while in others, it may be associated with maternal infections, drug exposure, or other medical conditions that affect kidney development in the fetus.

The recurrence risk for Potter's syndrome in future pregnancies can vary depending on the underlying cause. If the condition is attributed to a specific genetic mutation, the recurrence risk may be higher, especially if both parents are carriers of the mutation. In such cases, genetic counseling and testing can be recommended to assess the risk and provide appropriate guidance.

However, if the cause of Potter's syndrome in the previous pregnancies is unknown or non-genetic, the chance of having three babies with the condition is generally considered to be low.

It's essential to consult with a medical professional, such as a geneticist or a high-risk pregnancy specialist, to understand the specific risk factors and recurrence probability based on the individual circumstances and medical history. They can provide personalized counseling and recommendations to manage the risks and plan for future pregnancies.