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Results 1 - 7 of 7 for Phenylketonuria
  1. 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 ...
  2. ... cases are caused by a similar condition called phenylketonuria (PKU). In certain countries, including Saudi Arabia, Taiwan, ...
  3. ... PAH gene have been identified in people with phenylketonuria (PKU). This condition increase the levels of phenylalanine ... Kensara OA. Genetic etiology and clinical challenges of phenylketonuria. Hum Genomics. 2022 Jul 19;16(1):22. ...
  4. ... known as mutations) in single genes, such as phenylketonuria (PKU), have high heritability. Most complex traits in ...
  5. ... pregnancy, and other maternal illnesses including diabetes and phenylketonuria. Although researchers are examining risk factors that may ...
  6. ... example of an inborn error of metabolism is phenylketonuria (PKU) . For other genetic conditions, treatment and management ...
  7. ... Nijmegen breakage syndrome Nonsyndromic hearing loss Pendred syndrome Phenylketonuria Primary hyperoxaluria Pyruvate kinase deficiency Rhizomelic chondrodysplasia punctata ...