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MLPA Subtelomere Analysis in Tunisian Mentally Retarded Patients
Subtelomeric rearrangements significantly contribute to idiopathic mental retardation and result in several mental retardation syndromes; however, most subtelomeric defects lack a characteristic phenotype. Thirty patients with unexplained mental retardation, a normal R banded karyotype at the 550 ba...
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Published in: | Biochemical genetics 2009-10, Vol.47 (9-10), p.727-733 |
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description | Subtelomeric rearrangements significantly contribute to idiopathic mental retardation and result in several mental retardation syndromes; however, most subtelomeric defects lack a characteristic phenotype. Thirty patients with unexplained mental retardation, a normal R banded karyotype at the 550 band, and no clinically recognizable syndrome were screened by Multiplex ligation-dependent probe amplification (MLPA). Four anomalies were identified: deletion 17q, duplications (4q), and associated duplications 15q and Xq. This duplication was found in two sisters of the proband. Anomalies were unidentified by the conventional technique. The prevalence of subtelomeric imbalances in our cohort of moderate to severe mental retardation is around 13% and is consistent with the literature. The sensitivity of the MLPA technique was characterized on cytogenetically verified positive and negative controls. MLPA is a fast, reliable, and relatively inexpensive technique to detect subtelomeric rearrangement in comparison with the fluorescence in situ hybridization (FISH) technique. |
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Thirty patients with unexplained mental retardation, a normal R banded karyotype at the 550 band, and no clinically recognizable syndrome were screened by Multiplex ligation-dependent probe amplification (MLPA). Four anomalies were identified: deletion 17q, duplications (4q), and associated duplications 15q and Xq. This duplication was found in two sisters of the proband. Anomalies were unidentified by the conventional technique. The prevalence of subtelomeric imbalances in our cohort of moderate to severe mental retardation is around 13% and is consistent with the literature. The sensitivity of the MLPA technique was characterized on cytogenetically verified positive and negative controls. MLPA is a fast, reliable, and relatively inexpensive technique to detect subtelomeric rearrangement in comparison with the fluorescence in situ hybridization (FISH) technique.</description><identifier>ISSN: 0006-2928</identifier><identifier>EISSN: 1573-4927</identifier><identifier>DOI: 10.1007/s10528-009-9271-1</identifier><identifier>PMID: 19590834</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>African Continental Ancestry Group - genetics ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Gene Deletion ; Gene Duplication ; Human Genetics ; Humans ; Intellectual Disability - genetics ; Karyotypes ; Medical Microbiology ; Nucleic Acid Amplification Techniques ; Phenotype ; Telomere ; Tunisia ; Zoology</subject><ispartof>Biochemical genetics, 2009-10, Vol.47 (9-10), p.727-733</ispartof><rights>Springer Science+Business Media, LLC 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-7b4171e6339f7d4b7d251e7271843c7d3f5d46c2ea12a40341ebae2bb1dfb9cc3</citedby><cites>FETCH-LOGICAL-c426t-7b4171e6339f7d4b7d251e7271843c7d3f5d46c2ea12a40341ebae2bb1dfb9cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19590834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hila, Lamia</creatorcontrib><creatorcontrib>Tébourbi, Hédia</creatorcontrib><creatorcontrib>Abaied, Leila</creatorcontrib><creatorcontrib>Rejeb, Imène</creatorcontrib><creatorcontrib>Ben Jemaa, Lamia</creatorcontrib><creatorcontrib>Chaabouni, Habiba</creatorcontrib><title>MLPA Subtelomere Analysis in Tunisian Mentally Retarded Patients</title><title>Biochemical genetics</title><addtitle>Biochem Genet</addtitle><addtitle>Biochem Genet</addtitle><description>Subtelomeric rearrangements significantly contribute to idiopathic mental retardation and result in several mental retardation syndromes; however, most subtelomeric defects lack a characteristic phenotype. Thirty patients with unexplained mental retardation, a normal R banded karyotype at the 550 band, and no clinically recognizable syndrome were screened by Multiplex ligation-dependent probe amplification (MLPA). Four anomalies were identified: deletion 17q, duplications (4q), and associated duplications 15q and Xq. This duplication was found in two sisters of the proband. Anomalies were unidentified by the conventional technique. The prevalence of subtelomeric imbalances in our cohort of moderate to severe mental retardation is around 13% and is consistent with the literature. The sensitivity of the MLPA technique was characterized on cytogenetically verified positive and negative controls. 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however, most subtelomeric defects lack a characteristic phenotype. Thirty patients with unexplained mental retardation, a normal R banded karyotype at the 550 band, and no clinically recognizable syndrome were screened by Multiplex ligation-dependent probe amplification (MLPA). Four anomalies were identified: deletion 17q, duplications (4q), and associated duplications 15q and Xq. This duplication was found in two sisters of the proband. Anomalies were unidentified by the conventional technique. The prevalence of subtelomeric imbalances in our cohort of moderate to severe mental retardation is around 13% and is consistent with the literature. The sensitivity of the MLPA technique was characterized on cytogenetically verified positive and negative controls. MLPA is a fast, reliable, and relatively inexpensive technique to detect subtelomeric rearrangement in comparison with the fluorescence in situ hybridization (FISH) technique.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>19590834</pmid><doi>10.1007/s10528-009-9271-1</doi><tpages>7</tpages></addata></record> |
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subjects | African Continental Ancestry Group - genetics Biochemistry Biomedical and Life Sciences Biomedicine Gene Deletion Gene Duplication Human Genetics Humans Intellectual Disability - genetics Karyotypes Medical Microbiology Nucleic Acid Amplification Techniques Phenotype Telomere Tunisia Zoology |
title | MLPA Subtelomere Analysis in Tunisian Mentally Retarded Patients |
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