4.2 Review

The genetics of cerebellar malformations

Journal

SEMINARS IN FETAL & NEONATAL MEDICINE
Volume 21, Issue 5, Pages 321-332

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.siny.2016.04.008

Keywords

Cerebellum; Neuroimaging; Magnetic resonance imaging; Genetics; Brain malformation; Neurodevelopment

Categories

Funding

  1. NIH [R01NS064077]

Ask authors/readers for more resources

The cerebellum has long been recognized for its role in motor co-ordination, but it is also increasingly appreciated for its role in complex cognitive behavior. Historically, the cerebellum has been overwhelmingly understudied compared to the neocortex in both humans and model organisms. However, this tide is changing as advances in neuroimaging, neuropathology, and neurogenetics have led to clinical classification and gene identification for numerous developmental disorders that impact cerebellar structure and function associated with significant overall neurodevelopmental dysfunction. Given the broad range in prognosis and associated medical and neurodevelopmental concerns accompanying cerebellar malformations, a working knowledge of these disorders and their causes is critical for obstetricians, perinatologists, and neonatologists. Here we present an update on the genetic causes for cerebellar malformations that can be recognized by neuroimaging and clinical characteristics during the prenatal and postnatal periods. (C) 2016 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available