Charcot-Marie-Tooth disease type 2G (CMT2G)

Pathology

• axonal degeneration

Genetics

• autosomal recessive
• associated with defects in GDAP1 gene

Clinical manifestations

• vocal paresis

Laboratory

• GDAP1 gene mutation

More general terms

• Charcot-Marie-Tooth disease type 2 (CMT2)

Database

• OMIM: https://mirror.omim.org/entry/607706