TREATMENTS &
RESEARCH

Search the
latest
treatment
information
here.

Dr. Huntley's
Diagnosis
Checklist

Have a symptom?
See what questions
a doctor would ask.
 
Dictionary » PKU
 

PKU

Introduction: PKU

Description of PKU

PKU (medical condition): A metabolic disorder where there is a deficiency of the enzyme phenylalanine hydroxylase which leads to a harmful buildup of the phenylalanine in the body. Normally the phenylalanine is converted into tyrosine. The severity of the symptoms can range from severe enough to cause mental retardation to mild enough not to require treatment. Severity is determined by the level of impairment of enzyme activity of phenylalanine hydroxylase.

See also:

Phenylketonuria:
  »Introduction: Phenylketonuria
  »Symptoms of Phenylketonuria
  »Tests for Phenylketonuria
  »Treatments for Phenylketonuria

PKU: Abbreviation for phenylketonuria.
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.

PKU as a Disease

PKU: Another name for Phenylketonuria (or close medical condition association).
  »Introduction: Phenylketonuria
  »Symptoms of Phenylketonuria
  »Treatments for Phenylketonuria

PKU: Related Diseases

PKU: PKU is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of PKU (Phenylketonuria)

Some of the symptoms of PKU incude:

See full list of 50 symptoms of PKU (Phenylketonuria)

Treatments for PKU (Phenylketonuria)

Treatments for PKU (Phenylketonuria) include:

  • Low-phenylalanine diet - a very strict diet to avoid particular substances.
    • Avoid high protein foods
    • Avoid aspartame - an artificial sweetener.
    • Avoid diet sodas - many contain aspartame
  • Strict diet during pregnancy - avoids damage to the fetus.

See full list of 6 treatments for PKU

Treatment of PKU: For more treatment information about PKU, see treatment of Phenylketonuria (PKU)

PKU: Article Excerpts about Phenylketonuria

Phenylketonuria (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase. (Source: Genes and Disease by the National Center for Biotechnology)

PKU: Related Disease Topics

These medical disease topics may be related to PKU:

Terms associated with PKU:

For a description of PKU, see:

Source: CRISP

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Late effects of tuberculosis of bones and joints
  • Late effects of tuberculosis of other specified organs
  • Late effects of unspecified accident
  • Late effects of viral encephalitis
  • Late endosomes
  • Late infant, not 'heavy-for-dates'
  • Late infantile MLD
  • Late latent syphilis
  • Late lesions of pinta
  • Late luteal phase dysphoria
  • Late luteal phase dysphoric disorder
  • Late metabolic acidosis of newborn
  • Late onset disorder

    Find out more

    Search to find out more about PKU:

      
      
    powered by
    Google

     » Next page: PKU type 1

    Rate This Website

    What do you think about the features of this website? Take our user survey and have your say:

    Website User Survey

    Medical Tools & Articles:

    Tools & Services:

    Medical Articles:

    Forums & Message Boards

  •  
    HONcode We subscribe to the HONcode principles

    By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

    Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise