Neonatal pancytopenia associated with de novo 1q43-44 deletion and 10p15 duplication

Inna Treskov, Mohamad Al-Hosni, Thomas G. Havranek, Jacqueline Batanian

Research output: Contribution to journalArticle

Abstract

Deletion of 1q43-44 has been reported in >50 cases. Phenotype-genotype correlation of this deletion has recently been described based on 20 pure cases. This led to the definition of critical regions and candidate genes for microcephaly, corpus callosum abnormalities, and seizure disorders. Variable penetrance and expressivity are associated with 1q43-44 microdeletion syndrome, explaining the lack of correlation in rare cases. Despite variation in size of the deletion, most cases are characterized by typical dysmorphic features, but none have demonstrated neonatal pancytopenia. We report on a newborn with partial monosomy 1q43-44 and partial trisomy 10p15.1→10pter born with dysmorphic features and neonatal pancytopenia. Array-CGH analysis characterizes the deletion and the duplication as terminal with estimated sizes of 8 to 9 and 5 to 6 Mb, respectively. Conventional cytogenetic analysis showed the 10p duplication as unbalanced and translocated onto 1q. The deletion in the 1q43-44 region is the largest among the 20 cases reported most recently. The 10p partnership with the derivative 1q43-44 region is unique. We discuss the association of neonatal pancytopenia with 1q deletion and 10p duplication, in light of a recent published case of acute lymphoblastic leukemia in a constitutional case of 1q deletion and 1p duplication.

Original languageEnglish (US)
JournalJournal of Pediatric Hematology/Oncology
Volume35
Issue number3
DOIs
StatePublished - Apr 2013
Externally publishedYes

Fingerprint

Pancytopenia
Microcephaly
Chromosome Deletion
Penetrance
Corpus Callosum
Cytogenetic Analysis
Trisomy
Genetic Association Studies
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Epilepsy
Genes
Trisomy 10p Chromosome 10

Keywords

  • 10p15
  • 1q43-44
  • Bone marrow failure syndrome
  • Microdeletion
  • Neonate
  • Pancytopenia
  • Partial trisomy
  • Unbalanced translocation

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Oncology
  • Hematology

Cite this

Neonatal pancytopenia associated with de novo 1q43-44 deletion and 10p15 duplication. / Treskov, Inna; Al-Hosni, Mohamad; Havranek, Thomas G.; Batanian, Jacqueline.

In: Journal of Pediatric Hematology/Oncology, Vol. 35, No. 3, 04.2013.

Research output: Contribution to journalArticle

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