The Canadian Journal of Neurological Sciences

Suppl. 1 – S38 moderate length-dependent polyneuropathy of axonal type. Detailed blood screening studies were negative. Genetic testing revealed the diagnosis of nail-patella syndrome with LMX1B gene mutation on chromosome 9q34. The lack of an identifiable acquired cause and the symmetric, slowly progressive and “painless” nature of the patient’s peripheral neuropathy point toward an inherited etiology. Conclusion: We present a case of slowly progressive sensorimotor axonal polyneuropathy in a patient with a diagnosis of NPS, which has not been previously reported. Peripheral nervous system disorder may be a variable phenotypic manifestation of LMX1B gene mutation.