Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings

• Published in: Gene 2013-03, Vol.517 (1), p.137-145
• Main Authors: Shojaei, Azadeh, Behjati, Farkhondeh, Derakhshandeh-Peykar, Pupak, Razzaghy-Azar, Maryam, Otukesh, Hasan, Kariminejad, Roxana, Dowlati, Mohammad-Ali, Rashidi-Nezhad, Ali, Tavakkoly-Bazzaz, Javad
• Format: Article
• Language: English
• Subjects: 13q Deletion; 7q Duplication; Abnormalities, Multiple - diagnosis; Abnormalities, Multiple - genetics; Array CGH; Child, Preschool; Chromosome Deletion; Chromosome Disorders - diagnosis; Chromosome Disorders - genetics; Chromosomes, Human, Pair 13 - genetics; Chromosomes, Human, Pair 7 - genetics; Comparative Genomic Hybridization; Disorders of sex development; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Male; Microcephaly; Oligonucleotide Array Sequence Analysis; Phenotype; Sexual Development - genetics; Translocation; Trisomy - diagnosis; Trisomy - genetics
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/j.gene.2012.11.013

Terminal 7q duplication and terminal 13q deletion are two conditions with variable phenotypes including microcephaly, thumb a-/hypoplasia, cortical dysplasia, microphtalmia, intellectual disability and dysmorphic features. We describe a boy born to a mother with a reciprocal t (7;13) who combines both a terminal 7q33-qter duplication and terminal 13q33-qter deletion through the inheritance of a derivative chromosome 13 (der (13)). The patient presented with developmental delay, facial and non-facial dysmorphic features, hypertonia, genital abnormality and skeletal malformation but no thumb a-/hypoplasia or microphtalmia. Knowing the exact breakpoints of his chromosomal aberrations using high resolution array CGH (aCGH) and comparison of his phenotypes with those of 24 and 59 previously published cases of 7q duplication and 13q deletion, respectively, allow us to further narrow the size of the proposed critical regions for microcephaly, thumb a-/hypoplasia and hypo/hypertonia on chromosome 13. ► We present a case with abnormal features born to a mother with a reciprocal t(7;13). ► Karyotype and MLPA showed both subtelomeric duplication of 7q and deletion of 13q. ► aCGH was used to narrow down the seeking region to the duplicated 7q/deleted 13q. ► A closer genotype/phenotype correlation is proposed.