Literature DB >> 20152051

"Idiopathic" mental retardation and new chromosomal abnormalities.

Cinzia Galasso1, Adriana Lo-Castro, Nadia El-Malhany, Paolo Curatolo.   

Abstract

Mental retardation is a heterogeneous condition, affecting 1-3% of general population. In the last few years, several emerging clinical entities have been described, due to the advent of newest genetic techniques, such as array Comparative Genomic Hybridization. The detection of cryptic microdeletion/microduplication abnormalities has allowed genotype-phenotype correlations, delineating recognizable syndromic conditions that are herein reviewed. With the aim to provide to Paediatricians a combined clinical and genetic approach to the child with cognitive impairment, a practical diagnostic algorithm is also illustrated. The use of microarray platforms has further reduced the percentage of "idiopathic" forms of mental retardation, previously accounted for about half of total cases. We discussed the putative pathways at the basis of remaining "pure idiopathic" forms of mental retardation, highlighting possible environmental and epigenetic mechanisms as causes of altered cognition.

Entities:  

Mesh:

Year:  2010        PMID: 20152051      PMCID: PMC2844383          DOI: 10.1186/1824-7288-36-17

Source DB:  PubMed          Journal:  Ital J Pediatr        ISSN: 1720-8424            Impact factor:   2.638


  44 in total

Review 1.  Monosomy 1p36 deletion syndrome.

Authors:  Marzena Gajecka; Katherine L Mackay; Lisa G Shaffer
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-11-15       Impact factor: 3.908

Review 2.  Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation.

Authors:  Pawel Stankiewicz; Arthur L Beaudet
Journal:  Curr Opin Genet Dev       Date:  2007-04-30       Impact factor: 5.578

Review 3.  Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis.

Authors:  Lisenka E L M Vissers; Bert B A de Vries; Joris A Veltman
Journal:  J Med Genet       Date:  2009-11-30       Impact factor: 6.318

Review 4.  Birth asphyxia and cerebral palsy.

Authors:  D M Hall
Journal:  BMJ       Date:  1989-07-29

5.  Autism, language delay and mental retardation in a patient with 7q11 duplication.

Authors:  C Depienne; D Heron; C Betancur; B Benyahia; O Trouillard; D Bouteiller; A Verloes; E LeGuern; M Leboyer; A Brice
Journal:  J Med Genet       Date:  2007-03-30       Impact factor: 6.318

Review 6.  Del 1p36 syndrome: a newly emerging clinical entity.

Authors:  Agatino Battaglia
Journal:  Brain Dev       Date:  2005-08       Impact factor: 1.961

Review 7.  The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future.

Authors:  Lisa G Shaffer; Bassem A Bejjani; Beth Torchia; Susan Kirkpatrick; Justine Coppinger; Blake C Ballif
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-11-15       Impact factor: 3.908

Review 8.  Chromosome 2q37 deletion: clinical and molecular aspects.

Authors:  Rena E Falk; Kari A Casas
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-11-15       Impact factor: 3.908

Review 9.  Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.

Authors:  Suzanne B Cassidy; Colleen A Morris
Journal:  Adv Pediatr       Date:  2002

10.  Diagnostic yield of the comprehensive assessment of developmental delay/mental retardation in an institute of child neuropsychiatry.

Authors:  A Battaglia; E Bianchini; J C Carey
Journal:  Am J Med Genet       Date:  1999-01-01
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  3 in total

Review 1.  Systematic review of central nervous system anomalies in incontinentia pigmenti.

Authors:  Snežana Minić; Dušan Trpinac; Miljana Obradović
Journal:  Orphanet J Rare Dis       Date:  2013-02-13       Impact factor: 4.123

2.  Multiplex ligation-dependant probe amplification study of children with idiopathic mental retardation in South India.

Authors:  Neetha John; Moka Rajasekhar; Katta Mohan Girisha; Podila Satya Venkata Narasimha Sharma; Puthiya Mundyat Gopinath
Journal:  Indian J Hum Genet       Date:  2013-04

3.  Screening for intellectual disability using high-resolution CMA technology in a retrospective cohort from Central Brazil.

Authors:  Rodrigo Roncato Pereira; Irene Plaza Pinto; Lysa Bernardes Minasi; Aldaires Vieira de Melo; Damiana Mirian da Cruz e Cunha; Alex Silva Cruz; Cristiano Luiz Ribeiro; Cláudio Carlos da Silva; Daniela de Melo e Silva; Aparecido Divino da Cruz
Journal:  PLoS One       Date:  2014-07-25       Impact factor: 3.240

  3 in total

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