Congenital hypothyroidism
Congenital hypothyroidism's disease overview
The thyroid gland is a butterfly -shaped endocrine gland with 2 lobes located in front of the neck. The thyroid uses iodine from the daily food to synthesize a hormone called T4 (thyroxine). T4 is an extremely important hormone for the development of the body, especially the brain.What is
What is congenital hypothyroidism?
congenital hypothyroidism is a condition that does not produce enough hormones to meet the body's necessary needs. The cause of birth defects without thyroid or hypothyroidism, minority or malformations due to defects of thyroid metabolism, or iodine deficiency, so it is impossible to synthesize the necessary Hormone T4 to meet sufficiently. Child's needs.
The thyroid hormone plays an important role in the function of living and intellectual and physical development in children. Therefore, if the hormone is lacking in the thyroid hormone, the child is not grown, the brain does not develop, the child becomes dwarf and the intellectual disability.In congenital hypothyroidism in newborns can be detected early by screening and treatment tests within 2 weeks after birth with hormonal drugs, children will develop completely. Normal. Therefore, screening tests should be performed in all children after birth.
The common incidence in the world is 1/4000 newborns living after birth. Women's/male incidence: 2/1
Children with congenital hypothyroidism at birth have vague symptoms, so parents are difficult to identify. Therefore, there is still a number of children diagnosed and treated late affecting the mental physical development of children. If the disease is detected and treated late after 3 months, the child will have a physical and mental retardation compared to his peers. Therefore, children need to be detected early and treated promptly.
The treatment is to supplement the daily thyroid hormone by lifetime orally every morning
Causes of Congenital hypothyroidism's disease
Symptoms of Congenital hypothyroidism's disease
The first phase of unclear symptoms is very difficult to detect, the symptoms of congenital hypothyroidism in the early stages are suspicious including the following symptoms:
Large first first
The later phase of symptoms may be more clear, but if these signs have just taken the child to the exam, it will be late to affect the child's brain because of the child's brain. Development very quickly in the first year developing 75% of adult brain.
Clinical signs of congenital hypothyroidism:
Short, thick neck, thick fat in the neck and shoulders.
Anemia: may appear
Prevention of Congenital hypothyroidism's disease
A diet of iodized salt supplements limits the incidence of disease
Diagnostic measures for Congenital hypothyroidism's disease
Diagnosis of congenital hypothyroidism is based on
Screening test
Neonatal screening: Use Test Test to assess TSH to help diagnose congenital hypothyroidism cases when the amount of TSH increases. Neonatal screening is the best measure to detect this disease early. 48 hours after birth, children will get heel blood to test TSH, if TSH increases, it is necessary to suspect congenital hypothyroidism and need more tests for diagnosis.
Diagnostic tests of congenital hypothyroidism
There is anti -hormone antibodies in the blood.
Imaging diagnostic: Imaging means to help diagnose the cause of congenital hypothyroidism:
XQ The left knee bone can help evaluate the development and formation of the young skeletal system
Congenital hypothyroidism's disease treatments
So can congenital hypothyroidism be cured?
Replace thyroid hormones with thyroxine. This is a synthetic hormone prepared into a tablet daily and lifelong use. It has very few side effects and if it is often due to the wrong use.
All children with congenital hypothyroidism must be clinically monitored and tested periodically.
See also:

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