The inheritance rate of fibroids

What is the inheritance rate of fibroids? Many people have misunderstandings about the inheritance rate of fibroids, so many young parents with fibroids dare not give birth easily, especially worried that their babies will inherit the disease. So today I will introduce to you, what is the inheritance rate of fibroids?

The chance of inheritance is very small. Similar inherited diseases will only occur when people have similar living habits. For example, if they like to eat the same food, are petty and sulky, and when the person's stomach and gallbladder are not in good condition, and when the positive energy cycle is weak, sulking will cause blockage of the gallbladder and stomach meridians in the breast, forming fibroids. If you pay attention to adjusting the function of your internal organs and your mood, you will not get fibroids.

Clinical manifestations are divided into the following categories according to the age of onset and the affected parts:

1. Juvenile fibromatosis occurs in children and young people.

2. Cervical fibromatosis refers to a type of fibromatosis that manifests at birth or shortly after birth and involves the lower 1/3 of the sternocleidomastoid muscle, sometimes bilaterally. Cervical fibromatosis is often accompanied by various congenital abnormalities.

3. Infant and young children's digital fibromatosis is a type of fibromatosis that usually occurs only in childhood. It typically occurs on the outer side of the finger (toe) tip, but can also occur in other parts of the body, such as the mouth and breast. This disease is often multiple and usually occurs at birth or within 2 years of age.

4. Infantile myofibromatosis is a solitary or multiple nodular lesion that occurs in the skin, soft tissue or bone. It can be confined to the above-mentioned parts or accompanied by the involvement of internal organs. The disease mostly occurs before the age of 2, and about 60% are congenital. The disease can also be seen in adults, with solitary cases more common in males and multiple cases more common in females. Familial cases are known, and evidence of autosomal dominant inheritance has been found.

5. Lipofibromatosis is a subtype of infantile fibromatosis, and local recurrence is common.

6. Multiple hyaline fibromatosis is a morphologically specific, familial multiple fibromatosis affecting children. It has no symptoms at birth and may be caused by congenital metabolic abnormalities.

7. Other cases include penile fibromatosis, palmar fibromatosis, plantar fibromatosis, scar fibromatosis and post-irradiation fibromatosis. Fibromatosis associated with multiple colon polyposis and occasionally multiple osteomas is called Gardner syndrome.