The phenotypic spectrum of trisomy 2: Report of two new cases

Ercan Mihci, Gopalrao V.N. Velagaleti, Regina Ensenauer, Dusica Babovic-Vuksanovic

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

We describe two cases of trisomy 2. The first case is a child with mosaic trisomy 2 who presented with mental retardation, multiple congenital anomalies, and dysmorphic findings similar to Pallister-Killian syndrome. The second case was an acardiac and acranial fetus with complete trisomy 2. We review the phenotypic spectrum associated with trisomy 2. Clin Dysmorphol 18:201-204.

Original languageEnglish (US)
Pages (from-to)201-204
Number of pages4
JournalClinical Dysmorphology
Volume18
Issue number4
DOIs
StatePublished - Oct 1 2009
Externally publishedYes

Keywords

  • Acardiac and acranial fetus
  • Mosaicism
  • Trisomy 2

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Anatomy
  • Pathology and Forensic Medicine
  • Genetics(clinical)

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