Ask what to look out for in hereditary polycystic kidney disease

In the case of cyst enlargement, some symptoms of compression can occur, and in severe cases, it can lead to a decrease in kidney function. It is recommended that you go to a professional urology department to check the CT and kidney function tests of the kidneys, and if there is obvious physical damage, you can choose minimally invasive surgery**.

The genetic probability of polycystic kidney disease is still quite large, if there is a polycystic kidney patient in both parents, the genetic probability is 50%, if both parents are polycystic kidney patients, the genetic probability is 75%, and the reason why the whole family is prone to this disease is that it is dominantly inherited, and the genetic probability accounts for half.

There is a 50% chance that one parent has polycystic kidney disease and a 75% chance that both parents have the disease.

Polycystic kidney disease is a hereditary disease, and the general genetic law is that if one of the parents has polycystic kidney disease, the hereditary rate is 75%, and if both parents have polycystic kidney disease, the heritability rate of the child is 50%. I'm a doctor plus 1597179300 can I elaborate on that.

Polycystic kidney disease is a hereditary disease, polycystic kidney disease follows the law of autosomal dominant inheritance, and the onset rate is equal in both males and females; The chance of one parent having the disease in their child is 50%, and if both parents have it, it increases to 75%. Symptoms do not appear until the cyst grows or increases in size, apparently squeezing the tissue surrounding the kidney cyst. Common first symptoms of polycystic kidney disease are high blood pressure, blood in the urine, abdominal pain, and sometimes a urinary tract infection or kidney stones.

Genetics depends on your condition.

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Polycystic kidney disease is a hereditary kidney disease, which is mainly manifested by multiple cysts of different sizes in both kidneys, and the cysts are progressively enlarged.

The disease is inherited in an autosomal dominant manner, and according to its inheritance law, it occurs from generation to generation, and the incidence of disease is equal for both men and women. If one parent is sick, the child has a 50% chance of getting sick. However, about 40% of patients have no family history of genetic inheritance, which may be caused by the patient's own genetic mutation.

Autosomal dominant polycystic kidney disease occurs between 1 in 1,000 and 2 in 1,000 in the population, and the incidence is the same for men and women; Children who do not have the disease do not carry the cyst gene, and if they marry the opposite sex without the disease, their children (grandchildren) will not develop the disease, that is, they will not be inherited from generation to generation; If one parent is sick, the incidence rate in children is about 50%, and if both parents are sick, the incidence rate rises to 75%. If both parents do not have the disease, the child has a genetic mutation, but this is very rare.

There are two types of polycystic kidney disease, autosomal recessive (infantile) polycystic kidney disease, which occurs in infancy; Autosomal dominant (adult) polycystic kidney disease, usually found in young middle age, can occur at any age. The incidence of autosomal dominant polycystic kidney disease ranges from 1 500 to 1000 people without gene decoding, while the incidence of autosomal recessive disease ranges from 1 200 to 40 000 people.

Characteristics of polycystic kidney disease: equal opportunities for both men and women; If one parent has polycystic kidney disease, 50% of the offspring will inherit the disease; If both parents have the disease, the incidence is 75% in offspring; Others are caused by genetic mutations.

Patient Consultation: Are Kidney Cysts Hereditary? Now it is multiple kidney cysts, it is said that it is very large, and it is necessary to surgically remove the whole cyst, it is a multiple cyst, a little hard, and one of them is removed.

She is very worried now, and she is also worried that her son and daughter will be inherited, so her son and daughter, who are now about 30 years old, how to judge whether their children will get the inheritance of polycystic kidney disease? Is this method to be judged first? Is there a way to do it, the expert replied:

Hello, parents are beloved sons, love their children, and hope that their children can be healthy, so when parents suffer from polycystic kidney disease, the most worried about their own condition is how to do it, but whether it will be passed on to their children, so we can understand the patient's mood, but I hope that patients do not worry too much, because polycystic kidney is not 100% genetic, and if it can be detected early in the early stage, it is possible to control the enlargement of the cyst and achieve cyst shrinkage. And in the later stage, you can have your own happy life with illness. In general, if one parent has polycystic kidneys, then the probability of a child having polycysts in the future will be 50% of the general population, and if both parents have polycystic kidneys, the probability of a child with polycystic kidneys will be greater. Therefore, in order to detect polycystic kidney disease early, it is recommended to do a B-ultrasound test every six months or a year, and a health examination every year if possible.

In this way, many small lesions can be detected early, early detection of early**, many diseases can be **, early kidney damage can be reversed, but it is very difficult in the late stage. In terms of life conditioning, avoid overeating, the taste of food should not be too strong, and life should be regular. So once polycystic kidney disease is diagnosed, it should be diagnosed as early as possible, so how should it be good?

Western medicine for polycystic kidney disease mainly adopts surgical methods, which is characterized by rapid effect and rapid reduction of the compression of renal cysts on the renal parenchyma, but there is great postoperative performance. Often, large cysts are small, small cysts are rapidly enlarged, and complications such as low back pain and high blood pressure may occur in the case of repeated conditions. Our hospital is conservative polycystic kidney, our miniaturized Chinese medicine penetrates the active substance has the effect of secreting intracystic fluid after the proliferation of epithelial cells on the inner wall of polycystic kidney cyst to effectively inhibit the secretion of intracystic fluid, the intracapsular pressure will be reduced, the cyst will shrink, and the pressure on the nephron will be reduced, which will fundamentally lead to polycystic kidney.

The content about "" is provided by professionals from Shijiazhuang Kidney Disease Hospital. For polycystic kidney disease, Shijiazhuang Kidney Disease Hospital not only created the original miniaturized Chinese medicine infiltration, but also fully integrated the most cutting-edge nephropathy technology to form the first technology of reversing the fluid difference in the cyst + controlling the shrinking of cysts + repairing and reconstructing kidney function. Polycystic kidney disease is properly controlled, and it is completely normal to live like a normal person.

Polycystic kidney disease is a hereditary disease, if one parent has polycystic kidney disease, the probability of inheritance in the next generation is 50%, if both parents have polycystic kidney disease, the probability of inheritance can reach about 75%. Polycystic kidney disease is dominantly inherited, not recessive, and may not necessarily be passed down from generation to generation, that is, it may not be passed from grandparents to parents, and then from parents to sons and grandchildren. Regardless of gender, as long as there is one generation without polycystic kidney disease, it will not be passed on to the next generation, so there is no need to worry too much about the genetic problems of polycystic kidney disease.

She may be observed for gross hematuria, which is due to a rupture of a blood vessel in the cyst wall. When bleeding is profuse, a blood clot passing through the ureter can cause cramping. Hematuria is often accompanied by leukocytouria and proteinuria, and the amount of protein in the urine is small, generally not more than a gram day.

Intrarenal infection is marked with pyuria, hematuria is aggravated, and flank pain is accompanied by fever.

Polycystic kidney disease is an inherited disease with a 50% chance of inheritance. It is characterized by familial clustering, which can occur in both sexes, with an equal chance of involvement in both sexes, and can occur in successive generations.

Analysis of relevant causative gene mutations should be performed as early as possible for the differential diagnosis of patients with early polycystic kidney disease. To avoid the delay caused by the late onset of disease symptoms, the decoding of accurate pathogenic gene identification genes can provide an effective and reliable basis for the differential diagnosis, search and pathogenesis of diseases, and avoid misdiagnosis and delay the best time to endanger the health of patients.

The cause of the disease can be determined through the identification of the pathogenic gene, and then the children can be verified to determine whether it is inherited.

Polycystic kidney disease is a congenital hereditary disease, which is mainly manifested by multiple or countless fluid cysts of different sizes in both kidneys, which makes the kidneys significantly enlarge and morphologically abnormal. As the disease progresses, the cyst can increase in size and eventually cause kidney failure due to severe damage to the kidney tissue.

The clinical symptoms of polycystic kidney failure are more complex, in addition to the characteristic changes of polycystic kidney such as low back pain, abdominal mass (enlarged kidney), hematuria, etc., many complications can also occur, such as hypertension, cyst infection, cyst rupture, etc., and in the late stage, abdominal distention, waist pain, dyspnea, urine infection, nausea and vomiting, etc., the patient is very painful.

For the occurrence and development of polycystic kidney failure, there is no effective one, but mainly to actively prevent the occurrence and development of polycystic kidney complications at an early stage, so as to protect the residual renal function and avoid further damage to renal function. As long as they can accept the correct and reasonable **, the clinical symptoms and kidney function of most patients can be controlled or improved, so that the condition is relatively stable, the quality of life is improved, and the life is prolonged.

Polycystic kidney disease is indeed likely to be inherited, the probability of polycystic kidney generally being inherited to the next generation is 50, if both parents are polycystic kidney patients, it may be nearly 100, so polycystic kidney patients do not get married, we must seriously consider the issue of offspring, in addition, the age of onset of polycystic kidney genetic patients is mostly between 30 and 40 years old, so polycystic kidney patients should pay attention to heredity and pay attention to time.

Under normal circumstances, patients with polycystic kidney disease will have medical instructions to remind patients to pay attention to relevant matters. The most important thing is to pay enough attention to your diet.

With the change of people's lifestyle, people's dietary requirements are getting higher and higher. The choice of diet is very important for patients with diseases, and the appropriateness of the patient's food is directly related to their own disease. What should a patient with so many cystic kidneys eat?

How to Eat Science for Patients with Polycystic Kidney Disease? Let's ask a nephrologist to introduce us to some of the issues that should be paid attention to in the diet of polycystic kidney disease:

Foods to eat for polycystic kidney patients:

1. Fruits and vegetables with high vitamins.

2. Iron-rich fruits and vegetables.

3. Vegetables and foods that can accommodate fossils.

4. Foods with diuretic effect.

Foods to avoid in patients with polycystic kidney disease:

1.The diet of polycystic kidney disease should pay attention to alcoholic beverages, alcohol, especially liquor, ......2.Don't eat fermented foods.

3.High-protein foods. For every kidney disease, a low-protein diet should be indicated. That is, to use a low-protein diet to match**.

4.Cooked food made from organ meats and animal offal is also not suitable for polycystic kidney patients.

5.In the diet of polycystic kidney, strong tea, coffee, chocolate cracked cherry blossoms, barbecue food, etc. are strictly prohibited.

6.Roasted meat, dried and salted food, etc.

Is polycystic kidney disease necessarily inherited? Many people with polycystic kidney disease have a family history, so is it necessarily hereditary? According to this, nephrologists at the Kidney Health Network call polycystic kidney disease a genetic disorder

According to the genetic characteristics, it is divided into two types: autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (hereditary polycystic kidney disease).

Is polycystic kidney disease necessarily inherited? If at least one parent has polycystic kidney disease, will the next generation of children inherit polycystic kidney disease? How should I get polycystic kidney disease? Is there a best way to do it?

Will polycystic kidney disease be passed on to the next generation? What are the chances of inheriting polycystic kidney disease? What should I do if I have polycystic kidney disease?

Is there a good way to do this? In this issue, we invite nephrologists from the Kidney Disease Health Network to introduce to you, hoping to help patients with polycystic kidney disease.

How does hereditary polycystic kidney disease**? Polycystic kidney disease is a hereditary kidney disease, so for patients with polycystic kidney disease, can they only wait for the onset of the disease and be helpless?

Polycystic kidney disease, most people are very vague about this concept when they first come into contact, generally speaking, the symptoms are not obvious, only occasional low back pain, but this small symptom is often ignored, many polycystic kidney patients are found in the inadvertent physical examination of polycystic kidney disease, and begin to slowly understand polycystic kidney disease. Many patients with polycystic kidney disease ask: Will polycystic kidney disease develop into kidney failure and uremia?

How can I stop polycystic kidney disease from progressing to kidney failure? Is there really no good way to do polycystic kidney? How to get out of the misunderstanding of polycystic kidney disease?

Polycystic kidney disease, most people are very vague about this concept when they first come into contact, generally speaking, the symptoms are not obvious, only occasional low back pain, but this small symptom is often ignored, many polycystic kidney patients are found in the inadvertent physical examination of polycystic kidney disease, and begin to slowly understand polycystic kidney disease. Many patients with polycystic kidney disease ask: Will polycystic kidney disease develop into kidney failure and uremia?

How can I stop polycystic kidney disease from progressing to kidney failure? Is there really no good way to do polycystic kidney? How to get out of the misunderstanding of polycystic kidney disease?