Dissection of partial 21q monosomy in different phenotypes: Clinical and molecular characterization of five cases and review of the literature

Edoardo Errichiello, Francesca Novara, Anna Cremante, Annapia Verri, Jessica Galli, Elisa Fazzi, Daniela Bellotti, Laura Losa, Mariangela Cisternino, Orsetta Zuffardi

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Background: Partial deletion of chromosome 21q is a very rare chromosomal abnormality associated with highly variable phenotypes, such as facial dysmorphic features, heart defects, seizures, psychomotor delay, and severe to mild intellectual disability, depending on the location and size of deletions. So far, three broad deletion regions of 21q have been correlated with the clinical phenotype. Results: We described the clinical and genetic features of three family members (father and two siblings) and other two unrelated patients with very wide range in age of diagnosis. All of them showed intellectual disability with very variable symptoms, from mild to severe, and carried 21q interstitial deletions with different sizes and position, as detected by conventional karyotype and array-CGH. Conclusions: Our study provided additional cases of partial 21q deletions, allowing to better delineate the genotype-phenotype correlations. In contrast to previous observations, we showed that deletions of the 21q proximal region are not necessarily associated with severe phenotypes and, therefore, that mild phenotypes are not exclusively related to distal deletions. To the best of our knowledge, this is the first report showing 21q deletions in adult patients associated with mild phenotypes, mainly consisting of neurobehavioral abnormalities, such as obsessive-compulsive disorders, poor social interactions and vulnerability to psychosis.

Original languageEnglish
Article number21
JournalMolecular Cytogenetics
Volume9
Issue number1
DOIs
Publication statusPublished - Feb 24 2016

Fingerprint

Dissection
Chromosome Deletion
Chromosomes
Phenotype
Defects
Intellectual Disability
Obsessive-Compulsive Disorder
Genetic Association Studies
Interpersonal Relations
Karyotype
Fathers
Chromosome Aberrations
Psychotic Disorders
Siblings
Seizures

Keywords

  • Array Comparative Genomic Hybridization (array-CGH)
  • Behavioral disorders
  • BTG3 (BTG family
  • DNA Copy Number Variations (CNVs)
  • GRIK1 (glutamate receptor
  • Intellectual Disability (ID)
  • Ionotropic
  • Kainate 1)
  • Member 3)
  • Partial 21q monosomy
  • RBM11 (RNA binding motif protein 11)

ASJC Scopus subject areas

  • Genetics
  • Molecular Biology
  • Genetics(clinical)
  • Biochemistry
  • Molecular Medicine
  • Biochemistry, medical

Cite this

Dissection of partial 21q monosomy in different phenotypes : Clinical and molecular characterization of five cases and review of the literature. / Errichiello, Edoardo; Novara, Francesca; Cremante, Anna; Verri, Annapia; Galli, Jessica; Fazzi, Elisa; Bellotti, Daniela; Losa, Laura; Cisternino, Mariangela; Zuffardi, Orsetta.

In: Molecular Cytogenetics, Vol. 9, No. 1, 21, 24.02.2016.

Research output: Contribution to journalArticle

Errichiello, E, Novara, F, Cremante, A, Verri, A, Galli, J, Fazzi, E, Bellotti, D, Losa, L, Cisternino, M & Zuffardi, O 2016, 'Dissection of partial 21q monosomy in different phenotypes: Clinical and molecular characterization of five cases and review of the literature', Molecular Cytogenetics, vol. 9, no. 1, 21. https://doi.org/10.1186/s13039-016-0230-3
Errichiello, Edoardo ; Novara, Francesca ; Cremante, Anna ; Verri, Annapia ; Galli, Jessica ; Fazzi, Elisa ; Bellotti, Daniela ; Losa, Laura ; Cisternino, Mariangela ; Zuffardi, Orsetta. / Dissection of partial 21q monosomy in different phenotypes : Clinical and molecular characterization of five cases and review of the literature. In: Molecular Cytogenetics. 2016 ; Vol. 9, No. 1.
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