Multiple respiratory complications in a patient with Charcot-Marie-Tooth disease with MFN2 mutation
Multiple respiratory complications in a patient with Charcot-Marie-Tooth disease with MFN2 mutation
Blog Article
Charcot-Marie-Tooth disease (CMT) is a Metalised Polypropylene hereditary peripheral neuropathy characterized by progressive atrophy of distal muscles.Respiratory complications are rare.We present a case of a 49-year-old male with childhood-onset CMT bearing a genetic mutation of MFN2.He had difficulty breathing when he was 46.
Imaging examination revealed complications of phrenic nerve paralysis and pneumothorax with a funnel chest.Respiratory function test demonstrated 624 severe restrictive ventilatory impairment.Polysomnography supported the diagnosis of mild sleep apnea syndrome.Noninvasive positive pressure ventilation successfully reduced respiratory symptoms.
To our knowledge, this is the first demonstration of multiple respiratory complications in a CMT patient.