Phenylketonuria screening: Difference between revisions

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{{Phenylketonuria}}
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{{CMG}}; {{AE}} [[User:Yanira Gavidia|Yanira Gavidia, M.D.]]
 
==Overview==
==Overview==
==Historical Perspective==
Newborns are usually screened for phenylketonuria between the age of 6 to 14 days using either HPLC or Guthrie test. If results are positive, the test is usually repeated at 2 weeks of age to confirm or rule out the diagnosis.
 
==Screening==
*Newborns are usually screened at day 6 to 14 following birth
*Neonatal heel prick is used to obtain a blood sample for screening.
*Screening for PKU is by usually either by [[HPLC]] test or by [[Guthrie test]].<ref name="pmid26025111">{{cite journal| author=Zerjav Tansek M, Groselj U, Angelkova N, Anton D, Baric I, Djordjevic M et al.| title=Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries. | journal=Orphanet J Rare Dis | year= 2015 | volume= 10 | issue= 1 | pages= 68 | pmid=26025111 | doi=10.1186/s13023-015-0283-0 | pmc=PMC4451731 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26025111  }} </ref>
*If a test result returns positive, the test is typically repeated at 2 weeks of age to confirm or rule out the diagnosis.
 
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
[[Category:Metabolic disorders]]
 
[[Category:Genetic disorders]]
[[Category:Congenital disorders]]
[[Category:Pediatrics]]
[[Category:Pediatrics]]
[[Category:Neurology]]
[[Category:Neurology]]
[[Category:Metabolism]]
[[Category:Endocrinology]]
[[Category:Inborn errors of metabolism]]
 
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Latest revision as of 13:12, 26 July 2016

Phenylketonuria Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Phenylketonuria from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

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Risk calculators and risk factors for Phenylketonuria

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Yanira Gavidia, M.D.

Overview

Newborns are usually screened for phenylketonuria between the age of 6 to 14 days using either HPLC or Guthrie test. If results are positive, the test is usually repeated at 2 weeks of age to confirm or rule out the diagnosis.

Screening

  • Newborns are usually screened at day 6 to 14 following birth
  • Neonatal heel prick is used to obtain a blood sample for screening.
  • Screening for PKU is by usually either by HPLC test or by Guthrie test.[1]
  • If a test result returns positive, the test is typically repeated at 2 weeks of age to confirm or rule out the diagnosis.

References

  1. Zerjav Tansek M, Groselj U, Angelkova N, Anton D, Baric I, Djordjevic M; et al. (2015). "Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries". Orphanet J Rare Dis. 10 (1): 68. doi:10.1186/s13023-015-0283-0. PMC 4451731. PMID 26025111.

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