What are the most common symptoms of phenylketonuria?
In many parts of the world, most people will never see common symptoms of PKU or phenylketonuria because many countries commonly test this genetic disorder in the first few days of life. Although the condition is unusual, this condition is when it is not treated, very serious and within a few months of birth can begin to cause serious lifelong side effects. Emphasis for testing every newborn is to ensure that those who have PKu will receive immediate treatment in the form of a low protein diet that lacks phenylalanins that otherwise build and cause damage. Early intervention is the key to preventing all symptoms of phenylketonuria and providing people to live relatively normal lives.
When this testing is not available or only optional, a number of symptoms of phenylketonuria in a child with a PKU will appear when the child is only a month or two months. Parents may notice that children have excessive diarrhea or vomiting, causing poor weight gain and can cause failure. GavePeople may seem much less obvious to people from the symptoms of phenylketonuria. Children can be sensitive to light, which is true for many children. Parents should look for excessive light sensitivity, but this may not be the best diagnostic factor.
A child with symptoms of phenylketonuria is also characterized as very harsh or difficult. Such children can cry much more often, which is sometimes rejected as how many. It is not so easy to reject persistent skin problems such as dryness or eczema that can be rich. In addition, children with PKU often have a special scent, which is described as almost musty or moldy. This odor may also be present in the urine and differ very much from the typical odor of the child.
If these symptoms of phenylketonuria are not recognized, the condition deteriorates within a few months. Growing levels of phenylalanins in points that cannot be broken or excreted will begin to cause weightbrain damage. This could be expressed by the failure of any or all developmental milestones, self -harmful behavior, such as the banging of the head, the growing retardation that can quickly become deep and the occurrence of seizures. The emergence of these symptoms is usually an indication of PKU, but hopefully its earlier indications led to treatment.
When the symptoms of phenylketonuria are recognized early, it is possible to prevent the difficult challenges that people with undiagnosed PKu face the difficult challenges. Although a diet without phenylalanine may be restrictive, it usually means that a person who is on such a diet after early diagnosis does not suffer from the extremes of PKu. Knowledge remains strong, developmental milestones are achieved in time and there are few disabilities. This is undoubtedly the best argument for the soon diagnosis. It is highly desirable to handle this condition before damage begins to increase.