Phenylketonuria - Medicow
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Topic: Phenylketonuria



  
 Phenylketonuria
Burgard, P. "Development of intelligence in early treated phenylketonuria." European Journal of Pediatrics 159, Suppl.
"Behaviour in early treated phenylketonuria: a systematic review." European Journal of Pediatrics 159, no. 14 (2000): S89-93.
"Review: Patterns of academic achievement among patients treated early with phenylketonuria." European Journal of Pediatrics 159, no.14 (2000): S96-9.
http://www.lifesteps.com/gm/Atoz/ency/phenylketonuria.jsp   (3120 words)

  
 [No title]
Related concepts: PKU, Classic phenylketonuria, Benign hyperphenylalaninemia, Malignant hyperphenylalaninemia, Transient hyperphenylalaninemia.
Includes general information about the condition, dietary advice, research, personal stories and support.
Basic Information Phenylketonuria (PKU) is a rare, genetic disorder that affects the body's metabolic system.
http://www.diseasedirectory.net/Rare_Disorders/Phenylketonuria/default.aspx   (411 words)

  
 Dr. Koop - Phenylketonuria- Health Encyclopedia and Reference
You should promptly seek professional medical care if you have any concern about your health, and you should always consult your physician before starting a fitness regimen.
Phenylketonuria (PKU) is a metabolic disorder caused by a deficiency of the enzyme phenylalanine hydroxylase.
Prospective mothers who have PKU should be started on a low-phenylalanine diet before conception, and every effort should be made to keep blood levels low throughout pregnancy.
http://www.drkoop.com/encyclopedia/43/560.html   (566 words)

  
 phenylketonuria - definition of phenylketonuria in Encyclopedia
Phenylketonuria was discovered by the Norwegian physician Ivar Asbjørn Følling, in 1934, when he noticed that hyperphenylalanemia (HPA) was associated with mental retardation.
Phenylketonuria "fee-nil-kee-ton-yur-ee-aah"+ (PKU) is a human genetic disorder that occurs in about 1 in 15,000 births, but the incidence varies widely in different human populations from 1 in 4,500 births among the Irish to fewer than one in 100,000 births among the population of Finland.
The sweat and urine of an affected child has a musty odour due to these ketones.
http://encyclopedia.laborlawtalk.com/phenylketonuria   (532 words)

  
 Darien Library: Health
Covers well known disorders including Down Syndrome, Trisomy, Hemophilia, and Tourette Syndrome and rarely seen diseases such as Meckel Syndrome, Neuraminidase Deficiency and Phenylketonuria.
http://www.darienlibrary.org/dataweb/health.php   (447 words)

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