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Title: Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
Author(s): Koolen, D.A. (298208490)
Nillesen, W.M.
Versteeg, M.H. (314285377)
Merkx, G.F.M.
Knoers, N.V.A.M. (298974460)
Kets, M. (298208644)
Vermeer, S. (314345027)
Ravenswaaij-Arts, C.M.A. van (230344143)
Kovel, C.G.F. de
Brunner, H.G. (112228682)
Smeets, D.F.C.M. (094500436)
Vries, L.B.A. de (157142396)
Sistermans, E.A. (14900107X)
Publication year: 2004
Document type: Article / Letter to editor
Journal: Journal of Medical Genetics
ISSN: 1468-6244
Volume: vol. 41
Issue: iss. 12
Start page: p. 892
End page: p. 899
Abstract: BACKGROUND: Subtelomeric rearrangements contribute to idiopathic mental retardation and human malformations, sometimes as distinct mental retardation syndromes. However, for most subtelomeric defects a characteristic clinical phenotype remains to be elucidated. OBJECTIVE: To screen for submicroscopic subtelomeric aberrations using multiplex ligation dependent probe amplification (MLPA). METHODS: 210 individuals with unexplained mental retardation were studied. A new set of subtelomeric probes, the SALSA P036 human telomere test kit, was used. RESULTS: A subtelomeric aberration was identified in 14 patients (6.7%) (10 deletions and four duplications). Five deletions were de novo; four were inherited from phenotypically normal parents, suggesting that these were polymorphisms. For one deletion, DNA samples of the parents were not available. Two de novo submicroscopic duplications were detected (dup 5qter, dup 12pter), while the other duplications (dup 18qter and dup 22qter) were inherited from phenotypically similarly affected parents. All clinically relevant aberrations (de novo or inherited from similarly affected parents) occurred in patients with a clinical score of >or=3 using an established checklist for subtelomeric rearrangements. Testing of patients with a clinical score of >or=3 increased the diagnostic yield twofold to 12.4%. Abnormalities with clinical relevance occurred in 6.3%, 5.1%, and 1.7% of mildly, moderately, and severely retarded patients, respectively, indicating that testing for subtelomeric aberrations among mildly retarded individuals is necessary. CONCLUSIONS: The value of MLPA is confirmed. Subtelomeric screening can be offered to all mentally retarded patients, although clinical preselection increases the percentage of chromosomal aberrations detected. Duplications may be a more common cause of mental retardation than has been appreciated.
Subject: UMCN 1.2: Molecular diagnosis, prognosis and monitoring
Organization: Human Genetics
IQ Healthcare
Organization (former): Centre for Quality of Care Research
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/57521

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