Copyright © Philip M. Parker, INSEAD. Terms of Use.

Phenylketonuria

Definition: Phenylketonuria

Phenylketonuria

Noun

1. A genetic disorder of metabolism; lack of the enzyme needed to turn phenylalanine into tyrosine results in an accumulation of phenylalanine in the body fluids which causes various degrees of mental deficiency.

Source: WordNet 1.7.1 Copyright © 2001 by Princeton University. All rights reserved.
 


Synonym: Phenylketonuria

Synonym: PKU (n). (additional references)

Top     

Specialty Definition: Phenylketonuria

(From Wikipedia, the free Encyclopedia)

Phenylketonuria (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.

PKU usually is caused by a defective gene for the enzyme phenylalanine hydroxylase (PAH). It is inherited as an autosomal recessive trait. A rarer form of the disease occurs when PAH is normal but its cofactor tetrahydrobiopterin (BH4) is not synthesised by the patient.

This enzyme normally converts the amino acid phenylalanine to tyrosine. If, due to a faulty or missing enzyme, this reaction does not take place, levels of phenylalanine in the body can be far higher than normal, and levels of tyrosine lower than normal. Excess phenylalanine in the blood harms brain development in the child, leading to mental retardation; low levels of tyrosine leads to lowered production of the pigment melanin, so children with this condition tend to be fair haired and blue eyed. The excess phenylalanine is converted instead into phenylketones, which are excreted in the urine - hence the name for this condition. The sweat and urine of an affected child has a musty odour due to these ketones.

The problem is readily detectable within days of birth from a small blood sample -- the Guthrie heel prick test, so screening for phenylketonuria is done routinely in most industrialised countries, usually combined with testing thyroid function and other genetic disorders of metabolism. If the condition is diagnosed early enough, an affected child can grow up with normal brain development, by eating a special diet low in phenylalanine. In those patients with a deficit in BH4 production, treatment consists of giving this cofactor as a supplement.

External links

http://www.ehendrick.org/healthy/00060590.html
http://www.ultranet.com/~jkimball/BiologyPages/P/Phenylketonuria.html

Source: adapted by the editor from Wikipedia, the free encyclopedia under a copyleft GNU Free Documentation License (GFDL) from the article "Phenylketonuria."

Top     

Crosswords: Phenylketonuria

English words defined with "phenylketonuria": PKU test. (references)
Specialty definitions using "phenylketonuria": Phenylalanine Hydroxylase. (references)

Top     

Commercial Usage: Phenylketonuria

DomainTitle

References

  

Books

  • Phenylketonuria and some other inborn errors of amino acid metabolism: biochemistry, genetics, diagnosis, therapy (reference)

  • Practical Developments in Inherited Metabolic Disease: DNA Analysis, Phenylketonuria and Screening for Congenital Adrenal Hyperplasia (reference)

    (more book examples)

Source: compiled by the editor from various references; see credits.

Top     

Photo Album: Phenylketonuria

ThumbnailDescription & Credit

Blood taken is usually screened for Phenylketonuria (PKU), HIV, and cystic fibrosis, to name only a few disease processes that are detectable in this manner.Credit: CDC.

Source: compiled by the editor from various references; see credits.

Top     

Non-Fiction Usage: Phenylketonuria

SubjectTopicQuote

Health

In a minority of cases, disorders such as fragile X syndrome, tuberous sclerosis, untreated phenylketonuria (PKU), and congenital rubella cause autistic behavior. (references)

Classical phenylketonuria (PKU) is a rare metabolic disorder (and orphan disease) that usually results from a deficiency of a liver enzyme known as phenylalanine hydroxylase (PAH). (references)

It may occur in association with spinal cord injury, multiple sclerosis, cerebral palsy, anoxic brain damage, brain trauma, severe head injury, some metabolic diseases such as adrenoleukodystrophy, and phenylketonuria. (references)

Source: compiled by the editor from ICON Group International, Inc.; see credits.

Top     

Usage Frequency: Phenylketonuria

"Phenylketonuria" is generally used as a noun (singular) -- approximately 100.00% of the time. "Phenylketonuria" is used about 50 times out of a sample of 100 million words spoken or written in English. Its rank is based on over 700,000 words used in the English language. Some parts-of-speech are not covered due to the samples used by the British National Corpus. (note: percents less than one-hundredth of one percent have been omitted)
Parts of SpeechPercentUsage per
100 Million Words
Rank in English
Noun (singular)100%5048,117

Source: compiled by the editor from several corpora; see credits.

Top     

Frequency of Internet Keywords: Phenylketonuria

The following statistics estimate the number of searches per day across the major English-language search engines as identified by various trade publications. Hyperlinks lead to commercial use of the expression at Amazon.com.
 
ExpressionFrequency
per Day

  phenylketonuria

444

  phenylketonuria pku

5

  phenylalanine phenylketonuria

4

  phenylketonuria picture

4

  contains phenylalanine phenylketonuria

3

  phenylketonuria symptom

2
Source: compiled by the editor from various references; see credits.

Top     

Modern Translations: Phenylketonuria

Language Translations for "phenylketonuria"; alternative meanings/domain in parentheses.

Danish

  

phenylketonuria, oligophrenia phenylpyrouvica. (various references)

   

Dutch

  

phenylketonurie, phenylketonuria. (various references)

   

French

  

phénylcétonurie. (various references)

   

German

  

Phenylurie, Phenylketonurie. (various references)

   

Italian

  

fenilchetonuria. (various references)

   

Japanese Kanji 

  

フェニルケトン尿症 . (various references)

   

Japanese Katakana 

  

フェニルケトンにょうしょう. (various references)

   

Pig Latin

  

enylketonuriaphay

Source: compiled by the editor from various translation references.

Top     

Derivations: Phenylketonuria

Derivations

Words beginning with "phenylketonuria": phenylketonurias. (additional references)

Source: compiled by the editor, based on several corpora (additional references).

Top     

Anagrams: Phenylketonuria

Scrabble® Enable2K-Verified Anagrams

Words within the letters "a-e-e-h-i-k-l-n-n-o-p-r-t-u-y"

-3 letters: polyurethane.

-5 letters: anopheline, enkephalin, euphoriant, euryhaline, hypertonia, inherently, leukopenia, nalorphine, neuropathy, neutrophil, peritoneal.

 Words containing the letters "a-e-e-h-i-k-l-n-n-o-p-r-t-u-y"
 

+1 letter: phenylketonurias.

Source: compiled by the editor from various references; see credits.

SCRABBLE® is a registered trademark. All intellectual property rights in and to the game are owned in the U.S.A and Canada by Hasbro Inc., and throughout the rest of the world by J.W. Spear & Sons Limited of Maidenhead, Berkshire, England, a subsidiary of Mattel Inc. Mattel and Spear are not affiliated with Hasbro.

Top     

Alternative Orthography: Phenylketonuria


Hexadecimal (or equivalents, 770AD-1900s) (references)

50 68 65 6E 79 6C 6B 65 74 6F 6E 75 72 69 61

Leonardo da Vinci (1452-1519; backwards) (references)

American Sign Language (origins from 1620-1817 in Italy and, especially, France) (references)

=

Semaphore (1791, in France) (references)

Braille (1829, in France) (references)

Morse Code (1836) (references)

.--.    ....    .    -.    -.--.    .-..    -.-    .    -    ---    -.    ..-    .-.    ..    .-

Dancing Men (Sir Arthur Conan Doyle, 1903) (references)

Top     

 

Bibliographic Items: "phenylketonuria"


Top     

Amazon.com BOOKS: Search for: "phenylketonuria"

Top     

Public Service or Web Sites Triggered by: Phenylketonuria