17q12 Deletion in a patient with Williams syndrome: Case report and review of the literature

Lilian Cohen, Joy Samanich, Quilu Pan, Lakshmi Mehta, Robert W. Marion

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Williams syndrome (WS) is a complex genomic disorder entailing distinctive facial dysmorphism, cardiovascular abnormalities, intellectual disabilities, unusual behavioral features, and a specific cognitive profile with considerable variability. Additional symptoms include endocrine abnormalities, renal anomalies and connective tissue disorders. We report a monozygotic twin patient with WS who presented with multicystic kidneys in the newborn period, and, in addition to the typical WS deletion at 7q11.23, was found to have a de novo 1.7 Mb deletion in the 17q12 region on microarray comparative genomic hybridization. The co-twin was selectively terminated at 23 wk of gestation after being diagnosed with bilateral multicystic dysplastic kidneys and anhydramnios. Review of the literature shows that deletion of chromosome 17q12, encompassing hepatocyte nuclear factor 1beta gene, is associated with cystic renal disease and is the first recurrent genomic deletion associated with maturity onset diabetes of the young. In addition, reports of female reproductive tract malformations and patients with neurocognitive or psychiatric phenotypes have recently been described. This review of the literature summarizes 47 other cases involving 17q12 deletions with wide variability in phenotype, possibly suggesting a contiguous gene syndrome. It is likely that the additional 17q12 deletion has played a role in modifying the phenotype in our patient. This case highlights the importance of using array comparative genomic hybridization in the clinical setting to uncover the etiology of atypical findings in individuals with known microdeletion syndromes.

Original languageEnglish (US)
Pages (from-to)135-141
Number of pages7
JournalJournal of Pediatric Genetics
Volume1
Issue number2
DOIs
StatePublished - 2012

Fingerprint

Williams Syndrome
Multicystic Dysplastic Kidney
Comparative Genomic Hybridization
Phenotype
Hepatocyte Nuclear Factor 1-beta
Cardiovascular Abnormalities
Cystic Kidney Diseases
Chromosome Deletion
Monozygotic Twins
Intellectual Disability
Connective Tissue
Genes
Psychiatry
Newborn Infant
Kidney
Pregnancy

Keywords

  • 17q12 deletion
  • Genotype-phenotype correlation
  • Hepatocyte nuclear factor 1beta gene deletion
  • Microarray
  • Williams syndrome

ASJC Scopus subject areas

  • Genetics(clinical)
  • Pediatrics, Perinatology, and Child Health

Cite this

17q12 Deletion in a patient with Williams syndrome : Case report and review of the literature. / Cohen, Lilian; Samanich, Joy; Pan, Quilu; Mehta, Lakshmi; Marion, Robert W.

In: Journal of Pediatric Genetics, Vol. 1, No. 2, 2012, p. 135-141.

Research output: Contribution to journalArticle

Cohen, Lilian ; Samanich, Joy ; Pan, Quilu ; Mehta, Lakshmi ; Marion, Robert W. / 17q12 Deletion in a patient with Williams syndrome : Case report and review of the literature. In: Journal of Pediatric Genetics. 2012 ; Vol. 1, No. 2. pp. 135-141.
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