Rare copy number variants identified in prune belly syndrome

Details

• Alternative Title:
  Eur J Med Genet
• Personal Author:
  Boghossian, Nansi S. ; Sicko, Robert J. ; Giannakou, Andreas ; Dimopoulos, Aggeliki ; Caggana, Michele ; Tsai, Michael Y. ; Yeung, Edwina H. ; Pankratz, Nathan ; Cole, Benjamin R. ; Romitti, Paul A. ; Browne, Marilyn L. ; Fan, Ruzong ; Liu, Aiyi ; Kay, Denise M. ; Mills, James L.
• Description:
  Prune belly syndrome (PBS), also known as Eagle-Barrett syndrome, is a rare congenital disorder characterized by absence or hypoplasia of the abdominal wall musculature, urinary tract anomalies, and cryptorchidism in males. The etiology of PBS is largely unresolved, but genetic factors are implicated given its recurrence in families. We examined cases of PBS to identify novel pathogenic copy number variants (CNVs). A total of 34 cases (30 males and 4 females) with PBS identified from all live births in New York State (1998-2005) were genotyped using Illumina HumanOmni2.5 microarrays. CNVs were prioritized if they were absent from in-house controls, encompassed ≥10 consecutive probes, were ≥20 Kb in size, had ≤20% overlap with common variants in population reference controls, and had ≤20% overlap with any variant previously detected in other birth defect phenotypes screened in our laboratory. We identified 17 candidate autosomal CNVs; 10 cases each had one CNV and four cases each had two CNVs. The CNVs included a 158 Kb duplication at 4q22 that overlaps the BMPR1B gene; duplications of different sizes carried by two cases in the intron of STIM1 gene; a 67 Kb duplication 202 Kb downstream of the NOG gene, and a 1.34 Mb deletion including the MYOCD gene. The identified rare CNVs spanned genes involved in mesodermal, muscle, and urinary tract development and differentiation, which might help in elucidating the genetic contribution to PBS. We did not have parental DNA and cannot identify whether these CNVs were de novo or inherited. Further research on these CNVs, particularly BMP signaling is warranted to elucidate the pathogenesis of PBS.
• Subjects:
  Abdominal Wall Musculature Adult Article Copy Number Variant DNA Copy Number Variations Eagle-Barrett Syndrome Female Genotype Humans Infant, Newborn Male Phenotype Prune Belly Syndrome Sequence Analysis, DNA Young Adult

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• Source:
  Eur J Med Genet. 61(3):145-151
• Pubmed ID:
  29174092
• Pubmed Central ID:
  PMC5803418
• Document Type:
  Journal Article
• Funding:
  R01 DA024411/DA/NIDA NIH HHS/United States ; U01 DD001035/DD/NCBDD CDC HHS/United States ; HHSN275201100001I/HD/NICHD NIH HHS/United States ; WT_/Wellcome Trust/United Kingdom ; HHSN275201100001C/HD/NICHD NIH HHS/United States ; N01DK73431/HD/NICHD NIH HHS/United States ; HHSN275201100001G/HD/NICHD NIH HHS/United States
• Volume:
  61
• Issue:
  3
• Collection(s):
  CDC Public Access
• Main Document Checksum:
  urn:sha256:cd79af6befad3911363e5f9cfa8eb8b923d1fbdfbe2e6df657462670abf0d091
• Download URL:
  https://stacks.cdc.gov/view/cdc/82846/cdc_82846_DS1.pdf
• File Type:
  [PDF - 1.15 MB ]