How is infantile facial hemihypertrophy syndrome treated?

summary

Facial hemihypertrophy syndrome is Curtius I syndrome, also known as Steiner's syndrome, congenital partial hemihypertrophy of face, Friedreich's syndrome, ectodermal dysplasia ocular malformation syndrome, etc. It is a group of symptoms characterized by unilateral facial hypertrophy. Let's share my experience with you.

How is infantile facial hemihypertrophy syndrome treated?

After the development of the disease stopped naturally, the affected area could be corrected. Premarital physical examination plays a positive role in the prevention of birth defects. The size depends on the examination items and contents, mainly including serological examination (such as hepatitis B virus, Treponema pallidum, HIV), reproductive system examination (such as screening for Cervicitis), general physical examination (such as blood pressure, electrocardiogram), family history of diseases, personal past medical history, etc.

Pregnant women should avoid harmful factors as far as possible, including smoke, alcohol, drugs, radiation, pesticides, noise, volatile harmful gases, toxic and harmful heavy metals, etc. In the process of prenatal care during pregnancy, we need to carry out systematic birth defect screening, including regular ultrasound examination, serological screening, and if necessary, chromosome examination.

Once there are abnormal results, we need to know whether to terminate the pregnancy; The safety of fetus in uterus; Whether there are sequelae after birth, whether it can be treated, and how the prognosis is, etc. To take practical measures for diagnosis and treatment.

matters needing attention

In the diet must also control the salt intake, do not eat spicy food such as coffee, strong tea, you can eat more cereals such as cereals, oats or soybeans, you can drink more water or milk, but do not drink carbonated drinks.