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What is the treatment for phenylketonuria?

Anonymous

∙ 11y ago

Updated: 9/7/2023

The best treatment of phenylketonuria is a diet that is extremely low in phenylalanine during childhood. A person can also take fish oil supplements and iron supplements to help treat some of the symptoms.

Wiki User

∙ 11y ago

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Related Questions

What is phenylketonuria?

phenylketonuria

What is Phenylketonuria PKU?

phenylketonuria

What percentage of the world's population has phenylketonuria?

2.42% of the world's population has Phenylketonuria (pku)

What is the genetic disorder characterized by a missing digestive enzyme?

Phenylketonuria

Can Phenylketonuria treatment be stopped in adulthood?

Phenylketonuria (PKU) treatment typically involves a lifelong adherence to a low-phenylalanine diet and, in some cases, supplementation with amino acids. While some individuals may experience a reduction in dietary restrictions in adulthood, stopping treatment entirely is generally not recommended, as it can lead to neurodevelopmental issues and cognitive decline. It is essential for individuals with PKU to consult with healthcare professionals before making any changes to their treatment plan. Regular monitoring of phenylalanine levels is crucial to ensure health is maintained.

What has the author Virginia E Schuett written?

Virginia E. Schuett has written: 'Low protein cookery for phenylketonuria' -- subject(s): Recipes, Low-phenylalanine diet, Phenylketonuria, Low-protein diet, Diet therapy 'National survey of treatment programs for PKU and selected other inherited metabolic diseases' -- subject(s): Community health services, Directories, Directory, Disorders, Inborn Errors Metabolism, Metabolism, Metabolism, Inborn Errors, Phenylketonuria, Phenylketonurias, Puerto Rico, Statistics & numerical data, Therapy, Treatment, United States

Is phenylketonuria chromosmal?

peeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeeee

What is the abbreviation for phenylketonuria?

PKU

How long did it take to discover phenylketonuria?

Phenylketonuria is a genetic disorder that was first discovered in 1934 by Dr. Asbjorn Folling of Norway

Is phenylketonuria a learning disability?

Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.

What limitations do a person have if they have phenylketonuria?

your mother

What type of autosomal disease is phenylketonuria?

recessive

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