Clinical Case Reports · 2022 · 17 citations · 12 references
MedicineNeurologyPediatricsHuman GeneticsNeurogeneticsPediatric GeneticsGenetic DisordersVitamin E DeficiencyVitamin SupplementationAtaxia SyndromesAutosomal Dominant AtaxiaAutosomal Recessive InheritanceGenetic Disorders Of Vitamin MetabolismPediatric AtaxiaPediatric Vitamin E DeficiencyVitamin E SupplementationVitamin Metabolism Disorders
Ataxia with vitamin E deficiency (AVED) is a rare cause of hereditary ataxia in developing countries with unknown prevalence. AVED is an autosomal-recessive disorder, which is characterized by ataxia, areflexia, and proprioceptive and vibratory sensory loss. The disease is characterized clinically by symptoms with often resembling to those of Friedreich ataxia (FRDA). Vitamin E supplementation improves symptoms and prevents the progression of the disease. In this case report, we reviewed the recently updated findings in AVED in regard to the management and present a case of AVED in a 16-year-old boy, who was initially misdiagnosed as FRDA, prior to the genetic test.
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Vitamin E is essential for Purkinje neuron integrity
Lynn Ulatowski, Robert S. Parker, Govind Warrier et al. · Neuroscience · 2013 · 122 citations