MedicineNeurologyPediatricsNeurodegenerationNeuromuscular DisordersPediatric NeurologyGenetic DisordersNeurodevelopmental DisordersNeurogenetic DisordersPediatric Neurologic DisordersPediatric NeuropathologyAtaxia SyndromesNeurodegenerative GeneticsNeurologic DeficitsNeurologic DiagnosticsNeurological Status AssessmentNeurological Symptom AssessmentPediatric AtaxiaPediatric Neurological Assessment
Ataxia-telangiectasia (A-T) is a rare multisystem, neurodegenerative genetic disorder. We present a case of a 6-year-old girl who had a history of frequent respiratory infections and also had ocular and immunological features of this syndrome. The absence of neurological symptoms, which is very unusual for a patient of this age, raised many difficulties in the diagnosis of the disease. It is concluded that a normal neurological assessment must not exclude the diagnosis of A-T and delay the proper interventional measures.
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