Literature DB >> 15941363

Etiology of mental retardation in children referred to a tertiary care center: a prospective study.

Clara D M van Karnebeek1, Frederike Y Scheper, Nico G Abeling, Marielle Alders, Peter G Barth, Jan M N Hoovers, Cindy Koevoets, Ronald J A Wanders, Raoul C M Hennekam.   

Abstract

A prospective assessment following a step-wise protocol in 281 patients with unexplained cognitive delay was used to assess diagnostic possibilities. Diagnostic procedures were complex and required a multidisciplinary approach. One third of diagnoses was established based on clinical history and physical exam only; for another third, clinical history and physical exam provided essential clues for additional investigations; and a third were established by additional investigations only. The likelihood to reach a diagnosis did not depend on the severity of mental retardation. We found that in a tertiary care center, a diagnosis can be established in 1 out of every 2 patients. Clinical history and physical examination are the most important instruments to reach a diagnosis.

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Year:  2005        PMID: 15941363     DOI: 10.1352/0895-8017(2005)110[253:EOMRIC]2.0.CO;2

Source DB:  PubMed          Journal:  Am J Ment Retard        ISSN: 0895-8017


  16 in total

1.  Genomic Microarray in Intellectual Disability: The Usefulness of Existing Systems in the Interpretation of Copy Number Variation.

Authors:  Hela Ben Khelifa; Najla Soyah; Audrey Labalme; Helene Guilbert; Damien Sanlaville; Ali Saad; Soumaya Mougou-Zerelli
Journal:  J Pediatr Genet       Date:  2016-09-08

2.  Genetic Advances in Intellectual Disability.

Authors:  Donatella Milani; Luisa Ronzoni; Susanna Esposito
Journal:  J Pediatr Genet       Date:  2015-09

3.  Next-generation sequencing demands next-generation phenotyping.

Authors:  Raoul C M Hennekam; Leslie G Biesecker
Journal:  Hum Mutat       Date:  2012-03-27       Impact factor: 4.878

4.  Genetics of autism and mental retardation: A spoonful from the sea!

Authors:  Kanjaksha Ghosh; Ajit Gorakshakar
Journal:  Indian J Hum Genet       Date:  2009-09

5.  An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4.

Authors:  Kimia Kahrizi; Hossein Najmabadi; Roxana Kariminejad; Payman Jamali; Mahdi Malekpour; Masoud Garshasbi; Hans Hilger Ropers; Andreas Walter Kuss; Andreas Tzschach
Journal:  Eur J Hum Genet       Date:  2008-09-10       Impact factor: 4.246

Review 6.  Preventing abusive head trauma resulting from a failure of normal interaction between infants and their caregivers.

Authors:  Ronald G Barr
Journal:  Proc Natl Acad Sci U S A       Date:  2012-10-08       Impact factor: 11.205

7.  Study of inborn errors of metabolism in urine from patients with unexplained mental retardation.

Authors:  Angela Sempere; Angela Arias; Guillermo Farré; Judith García-Villoria; Pilar Rodríguez-Pombo; Lurdes R Desviat; Begoña Merinero; Angels García-Cazorla; Maria A Vilaseca; Antonia Ribes; Rafael Artuch; Jaume Campistol
Journal:  J Inherit Metab Dis       Date:  2010-01-05       Impact factor: 4.982

8.  High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?

Authors:  Laura Bernardini; Viola Alesi; Sara Loddo; Antonio Novelli; Irene Bottillo; Agatino Battaglia; Maria Cristina Digilio; Giuseppe Zampino; Adam Ertel; Paolo Fortina; Saul Surrey; Bruno Dallapiccola
Journal:  Eur J Hum Genet       Date:  2009-10-07       Impact factor: 4.246

9.  The treatable intellectual disability APP www.treatable-id.org: a digital tool to enhance diagnosis & care for rare diseases.

Authors:  Clara D M van Karnebeek; Roderick F A Houben; Mirafe Lafek; Wynona Giannasi; Sylvia Stockler
Journal:  Orphanet J Rare Dis       Date:  2012-07-23       Impact factor: 4.123

Review 10.  Metabolic evaluation of children with global developmental delay.

Authors:  So-Hee Eun; Si Houn Hahn
Journal:  Korean J Pediatr       Date:  2015-04-22
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