6-year-old phenylketonuria symptoms?

summary

Phenylketonuria is a common disease in newborns, such as the following symptoms, such as phenylketonuria can be detected by some examination methods. The common examination methods include bacterial inhibition test, blood phenylalanine determination, urine examination, amino acid chromatography, amino acid analysis, phenylalanine tolerance test, X-ray examination, Phenylketonuria in children brought about by the impact is more serious, phenylketonuria EEG examination 80% visible abnormalities, the following and everyone in detail to introduce, phenylketonuria differential diagnosis.

6-year-old phenylketonuria symptoms?

If there are other symptoms, consult the doctor in time, phenylketonuria differential diagnosis, phenylketonuria can be detected by some examination methods, the common examination methods are bacterial inhibition test, phenylalanine determination in blood, urine examination, amino acid chromatography, amino acid analysis, these methods can be used to differential diagnosis.

Phenylketonuria children after 1 year old motor development is also significantly backward, through understanding the disease, choose the appropriate method, for phenylketonuria this disease must be done, early detection and early treatment, early treatment effect is better, should match a corresponding treatment method, can achieve better treatment effect.

Phenylketonuria this disease is more common in newborns, in our daily life should also pay attention to diet conditioning, phenylketonuria to children's impact is more serious, phenylketonuria EEG examination 80% can see abnormal, phenylketonuria children generally will appear mental retardation, epilepsy is another feature of the disease.

matters needing attention

Phenylketonuria differential diagnosis, phenylketonuria can pass, always pay attention to, the condition can not be repeated at any time, check out the inspection method, common inspection methods are bacterial inhibition test, blood phenylalanine determination, urine examination, amino acid chromatography, amino acid analysis method, through these methods to differential diagnosis.