Ataxia-telangiectasia-like disorder

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.

Also known as: ATLD, ataxia - telangiectasia-like disorder, ataxia-telangiectasia-like disorder type 1, ATLD1, ataxia-telangiectasia-like disorder 1

1 clinical trial for this condition and its sub-types, 1 tagged with Ataxia-telangiectasia-like disorder itself.