Choroid plexus hyperplasia and monosomy 1p36: Report of new findings

Surasak Puvabanditsin, Eugene Garrow, Neisha Patel, Alexis D'Elia, Ahmed Zaafran, Nanthida Phattraprayoon, Suzanne Elizabeth Davis

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


Monosomy 1p36 is a newly delineated multiple congenital anomalies/mental retardation syndrome characterized by mental retardation, growth delay, epilepsy, congenital heart defects, characteristic facial appearance, and precocious puberty. It is now considered to be one of the most common subtelomeric micro-deletion syndromes. This article reports new findings of choroid plexus hyperplasia and dextrocardia with situs solitus in a patient who had deletion of chromosome 1p26.33 with a brief review of the literature.

Original languageEnglish (US)
Pages (from-to)922-925
Number of pages4
JournalJournal of Child Neurology
Issue number8
StatePublished - Aug 2008

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology


  • 1p36 deletion syndrome
  • Choroid plexus hyperplasia
  • Dextrocardia
  • Microdeletion
  • Monosomy 1p36


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