sei.pku.edu.cn
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1. Phenylketonuria (PKU) - Symptoms and causes - Mayo Clinic
Link: https://www.mayoclinic.org/diseases-conditions/phenylketonuria/symptoms-causes/syc-20376302
Description: May 13, 2022 · Phenylketonuria (fen-ul-key-toe-NU-ree-uh), also called PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to build up in the body. PKU is caused by a change in the phenylalanine hydroxylase (PAH) gene. This gene helps create the enzyme needed to break down phenylalanine.
DA: 22 PA: 16 MOZ Rank: 53
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2. Phenylketonuria (PKU): Symptoms, Causes & Treatment - Cleveland Clinic
Link: https://my.clevelandclinic.org/health/diseases/17816-phenylketonuria
Description: Aug 15, 2022 · Phenylketonuria (PKU) is a genetic condition that causes elevated levels of a substance called phenylalanine to build up in your body. Phenylalanine is found in the body as part of normal biochemical pathways, but problems …
DA: 59 PA: 65 MOZ Rank: 16
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3. Phenylketonuria - Wikipedia
Link: https://en.wikipedia.org/wiki/Phenylketonuria
Description: Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. Untreated PKU can lead to intellectual disability, seizures, behavioral problems, and mental disorders. It may also result in a musty smell and lighter skin.
DA: 26 PA: 72 MOZ Rank: 55
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4. Phenylketonuria: Causes, Symptoms, and Diagnosis - Healthline
Link: https://www.healthline.com/health/phenylketonuria
Description: Jul 25, 2017 · Prevention. What is phenylketonuria? Phenylketonuria (PKU) is a rare genetic condition that causes an amino acid called phenylalanine to build up in the body. Amino acids are the building...
DA: 46 PA: 33 MOZ Rank: 19
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5. Phenylketonuria (PKU) - Diagnosis and treatment - Mayo Clinic
Link: https://www.mayoclinic.org/diseases-conditions/phenylketonuria/diagnosis-treatment/drc-20376308
Description: May 13, 2022 · Phenylketonuria (PKU) Request an Appointment. Symptoms & causes. Diagnosis & treatment. Diagnosis. Newborn screening identifies almost all cases of phenylketonuria. All 50 states in the United States require newborns to be screened for PKU. Many other countries also routinely screen infants for PKU.
DA: 79 PA: 8 MOZ Rank: 85
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6. Phenylketonuria (PKU) - NICHD - Eunice Kennedy Shriver …
Link: https://www.nichd.nih.gov/health/topics/factsheets/pku
Description: May 15, 2012 · Phenylketonuria, often called PKU, is caused by phenylalanine hydroxylase (PAH) deficiency. It is an inherited disorder that can cause intellectual and developmental disabilities (IDDs) if not treated. In PKU, the body can’t process a portion of a protein called phenylalanine, which is in all foods containing protein.
DA: 13 PA: 63 MOZ Rank: 80
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7. About Phenylketonuria - National Human Genome Research …
Link: https://www.genome.gov/Genetic-Disorders/Phenylketonuria
Description: Aug 21, 2014 · Phenylketonuria (PKU) is an inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine. Phenylalanine comes from a person's diet and is used by the body to make proteins. Phenylalanine is found in all food proteins and in some artificial sweeteners.
DA: 30 PA: 45 MOZ Rank: 3
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8. Phenylketonuria: MedlinePlus Genetics
Link: https://medlineplus.gov/genetics/condition/phenylketonuria/
Description: Phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. Phenylalanine is a protein building block ( an amino acid) that is obtained from eating certain foods (such as meat, eggs, nuts, and milk) and in some artificial sweeteners.
DA: 68 PA: 23 MOZ Rank: 55
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9. Phenylketonuria - Symptoms, Causes, Treatment | NORD
Link: https://rarediseases.org/rare-diseases/phenylketonuria/
Description: Nov 17, 2023 · Phenylketonuria (PKU) is an inborn error of metabolism that can be diagnosed during the first days of life with routine newborn screening. PKU is characterized by absence or deficiency of an enzyme called phenylalanine hydroxylase (PAH), responsible for processing the amino acid phenylalanine.
DA: 34 PA: 11 MOZ Rank: 84
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10. About PKU - The National Society for Phenylketonuria (NSPKU)
Link: https://nspku.org/about-pku/
Description: Phenylketonuria (PKU) is a rare metabolic disorder. People with PKU cannot metabolise phenylalanine, an amino acid found in protein foods. This builds up to levels that are toxic to the brain. PKU is diagnosed by the “heel prick” new-born screening test. PKU is a treatable condition.
DA: 60 PA: 96 MOZ Rank: 86