Pontocerebellar hypoplasia: Review of classification and genetics, and exclusion of several genes known to be important for cerebellar development

Stephen M. Maricich, Kaashif A. Aqeeb, Yalda Moayedi, Erin L. Mathes, Millan S. Patel, David Chitayat, Gilles Lyon, Jules G. Leroy, Huda Y. Zoghbi

Research output: Contribution to journalReview articlepeer-review

Abstract

The pontocerebellar hypoplasias are a heterogeneous group of rare and devastating conditions characterized by multiple structural abnormalities of the ventral pons, inferior olive, and cerebellum. Here, we briefly review these conditions and discuss genes recently discovered to be involved in pontocerebellar hypoplasia pathogenesis. We then present data that exclude several genes important for cerebellar development as causes of pontocerebellar hypoplasia-4 and pontocerebellar hypoplasia-5, and we demonstrate that not all cases of clinically defined pontocerebellar hypoplasia-4 result from mutations in TSEN54. We conclude that classification based on clinical, imaging, and neuropathological findings does not differentiate between pontocerebellar hypoplasia subtypes with different genetic causes.

Original languageEnglish (US)
Pages (from-to)288-294
Number of pages7
JournalJournal of Child Neurology
Volume26
Issue number3
DOIs
StatePublished - Mar 2011

Keywords

  • aplasia
  • cerebellum
  • development
  • inferior olive
  • morphogenesis
  • pons
  • postocerebellar

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

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