Rinsho Shinkeigaku · 2017 · 10 citations · 21 references
MedicineNeurologyHuman GeneticsNeurogeneticsNeuromuscular DisordersGenetic DisordersInherited CardiomyopathiesMuscle DisordersMuscle PathologyNeurogenetic DisordersBilateral AsymmetryCardiopulmonary InvolvementGaitMuscle AtrophyNemaline MyopathyNeuromuscular Genetic DisordersSkeletal MyopathySteppage Gait
Nemaline myopathy commonly presents with symmetrical proximal weakness. Here we report two cases of nemaline myopathy presenting with distal dominant involvement with prominent asymmetry. Case 1 was a 37-year-old man who recalled frequently falling down and had right calf atrophy since he was 3-years-old. He had right calf muscle atrophy and weakness and steppage gait; his cardiopulmonary function was normal. Case 2 was a 35-year-old man with right calf muscle atrophy and weakness since childhood. He had right dominant distal leg weakness and atrophy together with respiratory failure and started noninvasive positive pressure ventilation. He also developed cardiomyopathy and died from acute respiratory failure due to pneumonia at age 39. Both cases harbored compound heterozygous nebulin (NEB) mutations with c.20131 C>T:p.Arg6711Trp and a nonsense mutation. Nemaline myopathy associated with NEB mutations can present as distal dominant myopathy with prominent asymmetry.
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Distal myopathy caused by homozygous missense mutations in the nebulin gene
Carina Wallgren‐Pettersson, Vilma‐Lotta Lehtokari, Hannu Kalimo et al. · Brain · 2007 · 147 citations · Full text
Life Sciences, Genetics, Neurology +13