Autosomal recessive spinocerebellar ataxia 20: Report of a new patient and review of literature.

Authors:
Anju Shukla, MD
Anju Shukla, MD
Sahara hospital
Histopathology
Lucknow, U.P | India

Eur J Med Genet 2017 Feb 29;60(2):118-123. Epub 2016 Nov 29.

Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India. Electronic address:

Inherited ataxias are an extremely heterogeneous group of disorders. Autosomal recessive spinocerebellar ataxia 20 (SCAR20) is a recently described disorder characterized by intellectual disability, ataxia, coarse facial features, progressive loss of Purkinje cells in the cerebellum and often hearing loss and skeletal abnormalities. Mutations in the gene SNX14, which plays an important role in autophagy, have been found to cause SCAR20. The unique clinical findings of progressive coarsening of facial features makes the clinical phenotype recognizable among the various hereditary ataxias. Here we report on a child with a novel missense mutation in the SNX14 gene that appears to be debilitating for protein conformation, function and review the previously reported cases from 15 families.

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Source
http://dx.doi.org/10.1016/j.ejmg.2016.11.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241222PMC
February 2017
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