Molecular Analysis Of A Constitutional Complex Genome Rearrangement With 11 Breakpoints Involving Chromosomes 3, 11, 12, And 21 And A Similar To 0.5-Mb Submicroscopic Deletion In A Patient With Mild Mental Retardation

Complex chromosome rearrangements (CCRs) are extremely rare but often associated with mental retardation, congenital anomalies, or recurrent spontaneous abortions. We report a de novo apparently balanced CCR involving chromosomes 3 and 12 and a two-way translocation between chromosomes 11 and 21 in a woman with mild intellectual disability, obesity, coarse facies, and apparent synophrys without other distinctive dysmorphia or congenital anomalies. Molecular analysis of breakpoints using fluorescence in situ hybridization (FISH) with region-specific BAC clones revealed a more complex character for the CCR. The rearrangement is a result of nine breaks and involves reciprocal translocation of terminal chromosome fragments 3p24.1 -> pter and 12q23.1 -> qter, insertion of four fragments of the long arm of chromosome 12: q14.1 -> 21?, q21?-> q22, q22 -> q23.1, and q23.1 -> q23.1 and a region 3p22.3 -> p24.1 into chromosome 3q26.31. In addition, we detected a similar to 0.5-Mb submicroscopic deletion at 3q26.31. The deletion involves the chromosome region that has been previously associated with Cornelia de Lange syndrome (CdLS) in which a novel gene NAALADL2 has been mapped recently. Other potential genes responsible for intellectual deficiency disrupted as a result of patient's chromosomal rearrangement map at 12q14.1 (TAFA2), 12q23.1 (METAP2), and 11p14.1 (BDNF).