Phenylalanine in diet soda: Is it harmful? - Mayo Clinic Phenylalanine is an amino acid, a building block of protein Most people don't need to worry about it But it is an issue for people who have a genetic condition called phenylketonuria (PKU) Genetic conditions are passed through families In people with PKU, phenylalanine can cause intellectual disability, brain damage, seizures, and skin and other problems Intellectual disability is slow
Phenylketonuria (PKU) - Symptoms and causes - Mayo Clinic A dangerous buildup of phenylalanine can develop when a person with PKU eats protein-rich foods, such as milk, cheese, nuts or meat, or grains such as bread and pasta, or aspartame, an artificial sweetener Inheritance For a child to inherit PKU, both the mother and father must have and pass on the changed gene
La fenilalanina en las gaseosas dietéticas: ¿puede ser perjudicial? En las personas con fenilcetonuria, la fenilalanina puede causar discapacidad intelectual, daño cerebral, convulsiones, problemas de la piel y de otro tipo La discapacidad intelectual es la lentitud en el aprendizaje y el desarrollo de habilidades La fenilalanina se encuentra en muchos alimentos ricos en proteínas, como la leche, los huevos y la carne La fenilalanina también se vende
Phenylketonuria (PKU) - Diagnosis and treatment - Mayo Clinic The phenylalanine-free formula provides essential protein (amino acids) and other nutrients in a form that's safe for people with PKU Your health care provider and dietitian can help you find the right type of formula Formula for babies and toddlers
الرعاية في مايو كلينك - Mayo Clinic المواعيد في Mayo Clinic تقدم Mayo Clinic المواعيد في كل من أريزونا وفلوريدا ومينيسوتا والمواقع الخاصة بالنظام الصحي المعمول به في Mayo Clinic
Loratadine (oral route) - Side effects dosage - Mayo Clinic Make sure you tell your doctor if you have any other medical problems, especially: Kidney disease or Liver disease—Use with caution Your dose must be determined by your doctor Phenylketonuria (PKU)—The chewable tablet contains phenylalanine (aspartame), which can make this condition worse
Fenilcetonuria - Síntomas y causas - Mayo Clinic A la fenilcetonuria la causa un cambio en el gen que ayuda a crear la enzima necesaria para descomponer la fenilalanina El tratamiento incluye principalmente una dieta especial y medicamentos
Cholestyramine (oral route) - Side effects dosage Phenylketonuria—Phenylalanine in aspartame is included in the sugar-free brand of cholestyramine and should be avoided Aspartame can cause problems in people with phenylketonuria
Sapropterin (oral route) - Side effects dosage - Mayo Clinic Sapropterin is used to lower phenylalanine levels in the blood of patients with phenylketonuria (PKU) High levels of phenylalanine (an amino acid) in the blood can cause severe brain damage, including intellectual disability, seizures, tremors, or decreased learning ability