Jul 6, 2022 · Ataxia-telangiectasia (A-T) is a rare genetic condition that affects the function of the nervous system, the immune system and several other body systems. Defining symptoms of A …

AT is caused by mutations in the ATM (ataxia-telangiectasis mutated) gene. Some children with AT develop cancer, most frequently acute lymphocytic leukemia or lymphoma. Neurological …

Ataxia–telangiectasia (AT or A–T), also referred to as ataxia–telangiectasia syndrome or Louis–Bar syndrome, [1] is a rare, neurodegenerative disease causing severe disability.

What is ataxia-telangiectasia? Ataxia-telangiectasia (AT) is a rare inherited condition that affects the nervous system, the immune system and other body systems.

Ataxia-telangiectasia is a rare inherited disorder that affects the nervous system, immune system, and other body systems. This disorder is characterized by progressive difficulty with …

People with A-T have trouble with movement and an increased risk of some types of cancer (see below). Children with A-T may begin staggering and appear unsteady (called ataxia) shortly …

What is ataxia telangiectasia? Ataxia telangiectasia (A-T) is a rare, inherited disease that affects several organs and systems, including the nervous and the immune systems. Most notably, it …

Aug 18, 2025 · Ataxia-telangiectasia (AT; MIM 208900) is an autosomal recessive disorder characterized by progressive cerebellar degeneration, oculocutaneous telangiectasia, …

Ataxia telangiectasia (A-T) is rare condition that affects the nervous system, the immune system, and many other parts of the body.

Aug 6, 2025 · Ataxia telangiectasia (AT) is a rare genetic condition that people inherit from their parents. AT affects the part of the brain that controls movement and coordination. Ataxia is …