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- W2016289080 abstract "We report a 7 year old girl who was evaluated for progressive thoracolumbar scoliosis and hypertrophic cardiomyopathy. Neurological examination was found to be abnormal and significant for absent reflexes and weakness distally in lower extremities and positive Romberg sign. Electromyogram showed length-dependent, axonal, sensorimotor polyneuropathy. Frataxin levels were low at 3ng/mL. Molecular testing for Friedreich ataxia showed significantly expanded GAA repeats at 799 (abnormal >67 GAA repeats) on one allele and a heterozygous disease causing mutation, c.317T>C (p.Leu106Ser) on the other allele, confirming the diagnosis. A review of Friedreich ataxia is provided in the case report." @default.
- W2016289080 created "2016-06-24" @default.
- W2016289080 creator A5047183629 @default.
- W2016289080 creator A5063844723 @default.
- W2016289080 date "2014-06-01" @default.
- W2016289080 modified "2023-09-25" @default.
- W2016289080 title "A 7-Year-Old Girl With Hypertrophic Cardiomyopathy and Progressive Scoliosis" @default.
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- W2016289080 doi "https://doi.org/10.1016/j.spen.2014.04.003" @default.
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