Ataxia-telangiectasia-like disorder 2

An autosomal recessive condition caused by mutation(s) in the MRE11A gene, encoding double-strand break repair protein MRE11. It is characterized by progressive cerebellar degeneration resulting in ataxia and oculomotor apraxia.

Disease Alternative Name

ataxia-telangiectasia-like disorder 1
ataxia-telangiectasia-like disorder
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