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Schematic view of the dominant X-linked inheritance pattern, the patient's mother (left) and the patient's father (right), who also follow CMT5 syndrome (CMTX).

Schematic view of the dominant X-linked inheritance pattern, the patient's mother (left) and the patient's father (right), who also follow CMT5 syndrome (CMTX).

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Figure 1: Human foot image of Charcot-Marie-Tooth syndrome with...
Figure 2: Images of related skeletal disorders in Charcot-Marie-Tooth...
Figure 4: Images of bone disorders in Charcot-Marie-Tooth syndrome.
Figure 5: Overview of Skeletal Disorders in the Legs and Hands of...
+15 Figure 6: Schematic overview of chromosome 17 where the PMP22 gene is...
The Role of Mutations in Genes PMP22, MPZ, LITAF, EGR2, NEFL, MFN2, KIF1B, RAB7A, LMNA, TRPV4, BSCL2, GARS, HSPB1, GDAP1, HSPB8, DNM2, PRX, MTMR2, SH3TC2, SBF2, NDRG1, FGD4, FIG4, YARS, GJB1, PRPS1, in Charcot-Marie-Tooth Syndrome
Article
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  • Feb 2020
Charcot-Marie-Tooth Disease (CMT; Charcot-Marie-Tooth) involves a large group of different forms of inherited motor (sen-sory) and sensory (sensory) neuropathies. The molecular basis of different CMT subtypes has been identified over the past 20 years. Because muscle weakness and sensory dysfunction that progresses slowly and slowly, the main chara...
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