Title: Distal limb deficiencies, micrognathia syndrome (OMIM 246560) and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements
Authors: Dimitrov, Boyan
de Ravel, Thomy
Van Driessche, J
de Die-Smulders, C
Toutain, A
Vermeesch, Joris
Fryns, Jean-Pierre
Devriendt, Koenraad
Debeer, Philippe # ×
Issue Date: Feb-2010
Publisher: BMJ Publishing Group
Series Title: Journal of Medical Genetics vol:47 issue:2 pages:103-111
Abstract: BACKGROUND: The 10q24 chromosomal region has previously been implicated in Split Hand Foot Malformation (SHFM). SHFM3 was mapped to a large interval on chromosome 10q. The corresponding Dactylaplasia mouse model was linked to the syntenic locus on chromosome 19. It was shown that the two existing Dac alleles result from MusD-insertions upstream of or within Dactylin (Fbxw4). However, all efforts to find the underlying cause for the human SHFM3 have failed on the anaysis of all the genes within the linkage region. Intriguingly a submicroscopic duplication within the critical locus on chromosome 10q24 was associated with the phenotype. METHODS AND RESULTS: As a part of screening for genomic rearrangements in cases with unexplained syndromic limb defects, a cohort of patients was analyzed by array CGH (Comperative Genomic Hybridization). A 10q24 microduplication was detected in 6 individuals with distal limb deficiencies associated with micrognathia, hearing problems and renal hypoplasia. In addition, in a family with two affected siblings, a somatic/gonadal mosaicism for the microduplication was detected in the apparently healthy mother. Using a high resolution oligoarray further delineation of the duplication size was performed. CONCLUSIONS: The detected 10q24 genomic imbalance in our syndromic patients has a similar size to the duplication in the previously reported individuals with an isolated form of SHFM, thus extending the clinical spectrum of SHFM3. These findings clearly demonstrate the importance of array CGH in the detection of the etiology of complex, clinically heterogeneous entities.
ISSN: 0022-2593
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Clinical Genetics
Clinical Genetics Section (-)
Orthopaedics Section (-)
Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

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