Redefined genomic architecture in 15q24 directed by patient deletion/ duplication breakpoint mapping

Ayman W. El-Hattab, Zhishuo Ou, Sung Hae L. Kang, Ankita Patel, Fernando Scaglia, James R. Lupski, Sau Wai Cheung, Pawel Stankiewicz, Teresa A. Smolarek, Martha E. Walker, Elizabeth K. Schorry, La Donna L. Immken, Gayle Patel, Mary Alice Abbott, Brendan C. Lanpher

Research output: Contribution to journalArticlepeer-review

60 Scopus citations


We report four new patients with a submicroscopic deletion in 15q24 manifesting developmental delay, short stature, hypotonia, digital abnormalities, joint laxity, genital abnormalities, and characteristic facial features. These clinical features are shared with six recently reported patients with a 15q24 microdeletion, supporting the notion that this is a recognizable syndrome. We describe a case of an ∼ 2.6 Mb microduplication involving a portion of the minimal deletion critical region in a 15-year-old male with short stature, mild mental retardation, attention deficit hyperactivity disorder, Asperger syndrome, decreased joint mobility, digital abnormalities, and characteristic facial features. Some of these features are shared with a recently reported case with a 15q24 microduplication involving the minimal deletion critical region. We also report two siblings and their mother with duplication adjacent and distal to this region exhibiting mild developmental delay, hypotonia, tapering fingers, characteristic facial features, and prominent ears. The deletion and duplication breakpoints were mapped by array comparative genomic hybridization and the genomic structure in 15q24 was analyzed further. Surprisingly, in addition to the previously recognized three low-copy repeat clusters (BP1, BP2, and BP3), we identified two other paralogous low-copy repeat clusters that likely mediated the formation of alternative sized 15q24 genomic rearrangements via non-allelic homologous recombination.

Original languageEnglish (US)
Pages (from-to)589-602
Number of pages14
JournalHuman genetics
Issue number4
StatePublished - 2009

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)


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