Late Onset of Severe Demyelinating Peripheral Neuropathy in a 62-Year-Old African American Woman

• Published in: Journal of clinical neuromuscular disease Vol. 25; no. 3; p. 152
• Main Authors: Zivkovic, Sasha A, DiCapua, Daniel
• Format: Journal Article
• Language: English
• Published: United States 01.03.2024
• Subjects: Black or African American; Carpal Tunnel Syndrome; Charcot-Marie-Tooth Disease - complications; Charcot-Marie-Tooth Disease - genetics; Female; Humans; Middle Aged; North American People
• ISSN: 1537-1611
• DOI: 10.1097/CND.0000000000000481

Hereditary neuropathies are typically associated with an early onset of symptoms, but same types of neuropathies may also manifest late, after the age 50 years. A 62-year-old African American woman presented with a 6-year history of gait unsteadiness and has been using a walker since the age 57 years after an unwitnessed fall. Gradual worsening of walking difficulties was later followed by decreased dexterity. The family history was negative for neuromuscular disorders, including neuropathy. On examination, the patient had both distal and proximal weakness with distal sensory loss to all modalities and hyporeflexia. Charcot Marie Tooth Examination Score was 12. Previous electrodiagnostic testing at the age 60 years showed severe sensorimotor demyelinating polyneuropathy with bilateral severe carpal tunnel syndrome. Genetic testing showed a homozygous pathogenic mutation in SH3TC2 gene (c.2860C>T; p.Arg954*), associated with CMT4C. CMT4C is the most common recessive demyelinating sensorimotor polyneuropathy and overall comprises 0.4%-1.7% of all patients with Charcot-Marie-Tooth disease. It is more common in French Canadians and Spanish Roma and in recent natural history study; only 1 of 56 patients was African American. This report demonstrates sporadic occurrence of CMT4C in other ethnic groups as well.