Re: screening of 4 new genetic diseases for newborn in Ji'nan can be reimbursed for 150 yuan.
phenylketonuria - endanger the nervous system
the disease is an autosomal recessive hereditary disease, endangering the nervous system, causing severe mental retardation and epilepsy in the children, and the malignant disease, except for mental retardation, and cerebral palsy, and the incidence of the disease is about 1:7800. Neonatal screening can be diagnosed early, and through long-term low phenylalanine diet control or drug treatment, the blood of children to reach a normal range of phenylalanine, children can normal development, the earlier the treatment time the better the better, more than 3 months without treatment will bring irreversible brain damage to the child.
s congenital hypothyroidism - commonly known as "dull"
this disease can lead to severe mental retardation and dwarfism, which is "low and silly", and the incidence is about 1:2000. The sooner the disease is found, the better the effect will be, and if the treatment begins within 3 months after birth, more than 80% of the children can reach the normal age of the same age.
/ > congenital adrenocortical hyperplasia -
abnormal
the disease mainly leads to sexual dysplasia. The loss of salt will endanger the life of the children. It is a set of congenital autosomal recessive hereditary diseases, the incidence of the disease is about 1:9500. The disease will lead to the hypofunction of the adrenal cortex and the abnormal increase of androgen level, which leads to the masculine masculine and masculine precocious puberty and the stature, which has a serious influence on the child's psychological and physiological development and the future work, marriage and birth. Screening and diagnosis can save lives and develop normal puberty after intervention.
glucose -6- phosphate dehydrogenase deficiency - erythrocyte enzyme deficiency
the disease is a hereditary erythrocyte enzyme deficiency with a incidence of about 1:3300. The disease can be diagnosed early by new screening, and measures can be taken to prevent the occurrence of nuclear jaundice in neonatal period, which can lead to low mental retardation in children, and prevent contact between the patients and the pathogenic factors and prevent the occurrence of adverse consequences.
free, how to avoid single
implement the reimbursement method after the first payment, the reimbursement standard is 150 yuan / person. The
reimbursement institution is designated by the county (city) District Maternal and child health care institution or the county (city) District Health Bureau. In principle, the mother's domicile is the place of reimbursement. The reimbursement time was 1 months after the screening of neonatal metabolic diseases. Specific list of reimbursement agencies can be found on the official website of Ji'nan Municipal Health Bureau.