Split hand/split foot malformation | Determining the frequency of genomic aberrations with molecular-genetic methods

Charlotte Ockeloen

ISBN 10: 3838125541 / ISBN 13: 9783838125541

Published by Südwestdeutscher Verlag für Hochschulschriften, 2015

About this Item

Split hand/split foot malformation | Determining the frequency of genomic aberrations with molecular-genetic methods | Charlotte Ockeloen | Taschenbuch | 68 S. | Englisch | 2015 | Südwestdeutscher Verlag für Hochschulschriften | EAN 9783838125541 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

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Bibliographic Details

• Title: Split hand/split foot malformation | Determining the frequency of genomic aberrations with molecular-genetic methods
• Publisher: Südwestdeutscher Verlag für Hochschulschriften
• Publication Date: 2015
• Language: English
• ISBN 10: 3838125541
• ISBN 13: 9783838125541
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 220W x 150H x 5D millimeters 220 millimeters width by 150 millimeters height by 5 millimeters depth
• Weight: 119 grams
• Seller catalogs:
  • Bücher

About this title

Synopsis

Split hand/split foot malformation (SHFM) is a mostly dominantly inherited congenital limb malformation. Until now, five genetic loci have been identified that contribute to the development of SHFM. Currently, TP63 mutation analysis (SHFM4) is the routine diagnostic test for SHFM. However, there are indications that the frequency of SHFM3 is substantially higher than that of SHFM4. So far, estimations of the frequency of the five known SHFM loci have not been made based exclusively on phenotype. In this study, 28 SHFM patients were analysed using array CGH, MLPA and qPCR to detect copy number variations at the five known genetic loci. TP63-positive patients were excluded. In our cohort, the frequency of SHFM3 was 25% (7/28). This result confirms our hypothesis that the frequency of SHFM3 in SHFM patients is substantially high and, in fact, about two times higher than the frequency of SHFM4, which is 10-15%. Therefore I recommend that in clinical practice patients with isolated SHFM should primarily be tested for copy number changes at the SHFM3 locus.

About the Author

Charlotte W. Ockeloen 16-03-1981 Clinical geneticist in training Radboud University Medical Centre Postbus 9101 6500 HB Nijmegen, the Netherlands Email: charlotteockeloen@hotmail.com