Hereditary axonal peripheral neuropathies comprise a genetically heterogeneous group of disorders that are clinically subsumed under the name of Charcot–Marie–Tooth (CMT) disease type 2 (CMT2).
We describe an unusual case of a woman in her 30s who had recently undergone Roux-en-Y gastric bypass and presented to the emergency department with a 6-week history of intractable nausea and vomiting ...
Primary genetic mitochondrial disorders arise from defects in either the mitochondrial or nuclear genome that impair mitochondrial function and structure. They are among the most common inborn errors ...
Vitamin B12 deficiency often affects the nerves in the extremities first, making the toes a common site for early warning signs. According to a study published in PubMed Central, B12 ...
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