Pontocerebellar Hypoplasia: Review of Classification and Genetics, and Exclusion of Several Genes Known to Be Important for Cerebellar Development

Author:

Maricich Stephen M.1,Aqeeb Kaashif A.2,Moayedi Yalda3,Mathes Erin L.4,Patel Millan S.5,Chitayat David6,Lyon Gilles7,Leroy Jules G.8,Zoghbi Huda Y.9

Affiliation:

1. Department of Pediatrics, Case Western Reserve University, Cleveland, OH, Departments of Neurosciences and Otolaryngology, Case Western Reserve University, Cleveland, OH

2. Department of Pediatrics, Baylor College of Medicine, Houston, TX

3. Department of Neuroscience, Baylor College of Medicine, Houston, TX

4. Department of Pediatrics, Case Western Reserve University, Cleveland, OH

5. Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada

6. Division of Clinical Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada

7. Department of Child Neurology, Hôpital R. Debré, University of Paris, France

8. Department of Medical Genetics, Antwerp University Hospital, Prins Boudewijnlaan, Antwerp, Belgium

9. Department of Pediatrics, Baylor College of Medicine, Houston, TX, Department of Neuroscience, Baylor College of Medicine, Houston, TX, Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, Howard Hughes Medical Institute, Chevy Chase, MD,

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.

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Reference31 articles.

1. Maricich SM, Zoghbi HY The cerebellum and the hereditary ataxias. In: In: Swaiman KF, Ashwal S, Ferriero DM, eds. Pediatric Neurology: Principles and Practice. 4th ed. Philadelphia : Mosby; 2006:1241-1269.

2. Pontocerebellar hypoplasias

3. Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene

4. Identification of Two Novel Human Putative Serine/Threonine Kinases, VRK1 and VRK2, with Structural Similarity to Vaccinia Virus B1R Kinase

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