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The Child with Developmental Delay: An Approach to Etiology

Overview
Specialty Pediatrics
Date 2009 Dec 17
PMID 20011550
Citations 5
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Abstract

Objective: To describe an approach to history, physical examination and investigation for the developmentally delayed child.

Methods: A review of electronic databases from 1997 to 2001 was done searching for articles relating to the approach to or investigations of children with developmental delay. Five studies, including a review of a consensus conference on evaluation of mental retardation, were chosen because of their general approaches to developmental delay and/or mental retardation, or specific evaluations of a particular laboratory investigation.

Conclusions: A diagnosis or cause of mental retardation can be identified in 20% to 60% of cases. Evaluation of the developmentally delayed child should include a detailed history and physical examination, taking special care to record a three-generation pedigree, as well as to look for dysmorphic features. If no other cause is apparent, routine investigations should include a chromosome study and fragile X studies. Further investigations are warranted depending on the clinical features.

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References
1.
White B, Ayad M, Fraser A, Entwistle T, Winkler S, Sbeiti A . A 6-year experience demonstrates the utility of screening for both cytogenetic and FMR-1 abnormalities in patients with mental retardation. Genet Test. 1999; 3(3):291-6. DOI: 10.1089/109065799316617. View

2.
Kotzot D . Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15. Am J Med Genet. 1999; 82(3):265-74. View

3.
Hunter A . Outcome of the routine assessment of patients with mental retardation in a genetics clinic. Am J Med Genet. 1999; 90(1):60-8. DOI: 10.1002/(sici)1096-8628(20000103)90:1<60::aid-ajmg11>3.0.co;2-p. View

4.
Curry C, Stevenson R, Aughton D, Byrne J, Carey J, Cassidy S . Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics. Am J Med Genet. 1997; 72(4):468-77. DOI: 10.1002/(sici)1096-8628(19971112)72:4<468::aid-ajmg18>3.0.co;2-p. View

5.
Hou J, Wang T, Chuang S . An epidemiological and aetiological study of children with intellectual disability in Taiwan. J Intellect Disabil Res. 1998; 42 ( Pt 2):137-43. DOI: 10.1046/j.1365-2788.1998.00104.x. View