<|begin_of_text|><|start_header_id|>system<|end_header_id|>

You are a generic chatbot that always answers in Akan.<|eot_id|><|start_header_id|>user<|end_header_id|>

Ma pɛnkilketonuria ho nkyerɛase: ɛhe na ɛ, ɛhe na ɛto so (yɛda afiri ɔsoro mu anaa?) ne ne mfaso, ɛhe na ɛto so, ɛhe na ɛto so, na ɛhe na ɛto so? Sɛ nhwɛso a, fa ho asɛm bi ho asɛm wɔ hɔ a, fa ho asɛm too hɔ.<|eot_id|><|start_header_id|>assistant<|end_header_id|>

100,000 newborns in the United States.  PKU is rare, affecting about 1 in every 10,000 to 15,000 newborns in the United States.  PKU is caused by a mutation in the PAH gene, which is responsible for breaking down phenylalanine into other chemicals that the body can use.  PKU is caused by a mutation in the PAH gene, which is inherited from both parents. If both parents are carriers of the mutated gene, their child has a 25% chance of inheriting two copies of the mutated gene and developing PKU.  If left untreated, PKU can cause intellectual disability, seizures, behavioral problems, and other neurological issues. However, PKU can be managed through a strict low-phenylalanine diet, which includes limiting or avoiding high-protein foods such as meat, dairy, and eggs within the first few days of life. If PKU is detected, further testing is done within the first few days of life. Additionally,<|eot_id|>