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PKU(short for Phenylketonuria) is a rare genetic disorder inherited from parents  which causes an amino acid called phenylalanine to build up in your body. This can lead to problems such a poor bone strength, intellectual disabilities, psychiatric disorders, as well as other health issues.
-https://www.mayoclinic.org/diseases-conditions/phenylketonuria/basics/definition/con-20026275

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Phenylketonuria or PKU is the most common congenital disorder affecting the metabolism of proteins. PKU is due to the mutation of a gene that codifies phenylalanine hydroxylase (PAH). If identified at birth, early treatment allows normal development and prevents any compromise of the central nervous system.

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PKU is caused by a defect in the gene that helps create the enzyme needed to break down phenylalanine.
https://www.mayoclinic.org/diseases-conditions/phenylketonuria/basics/definition/con-20026275

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http://www.aphlblog.org/2012/09/raising-baby-caroline-life-with-pku/

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Baby condition (risk):
- poor head growth
- delayed development
- heart defects

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Thanks to the generous philanthropic and volunteer support of our community, the Metabolic Camp at Emory University is able to make a difference in the lives of girls and women living with inherited metabolic disorders like PKU. You can make a gift of support to the Metabolic Camp at https://metcamp.net/donate .

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Low protein diet
- fruits
- vegetables
-  low-protein breads and cereals
- reduce amount of PHE in diet as much as possible
Medication
- Kuvan
https://www.mayoclinic.org/diseases-conditions/phenylketonuria/basics/treatment/con-20026275

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The purpose of this booklet is to inform you and your family of the importance of being on a low phenylalanine diet before and during pregnancy.