Screening for metabolic disorders: How are we doing?

M. Irons

doi:10.1016/S0031-3955(16)38624-2

Screening for metabolic disorders: How are we doing?

M. Irons^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

Abstract

Routine screening for phenylketonuria and congenital hypothyroidism has become an integral part of pediatric practice in the United States. Screening for several other metabolic disorders is now entering the second or third decade of use. New information is available for the pediatrician for both groups of disorders that will be of help in caring for children in the years to come.

Original language	English (US)
Pages (from-to)	1073-1085
Number of pages	13
Journal	Pediatric Clinics of North America
Volume	40
Issue number	5
DOIs	https://doi.org/10.1016/S0031-3955(16)38624-2
State	Published - 1993
Externally published	Yes

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

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10.1016/S0031-3955(16)38624-2

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title = "Screening for metabolic disorders: How are we doing?",

abstract = "Routine screening for phenylketonuria and congenital hypothyroidism has become an integral part of pediatric practice in the United States. Screening for several other metabolic disorders is now entering the second or third decade of use. New information is available for the pediatrician for both groups of disorders that will be of help in caring for children in the years to come.",

author = "M. Irons",

year = "1993",

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Screening for metabolic disorders: How are we doing?

Abstract

ASJC Scopus subject areas

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