Case report of a patient presenting both schizophrenia and Charcot-Marie-Tooth disease

Authors

  • Rym Rafrafi
  • Wafa Abdelaghaffar
  • Sami Ouanes
  • Imen Bekri
  • Wahid Melki
  • Zouhaier El Hechmi

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References

Ferrarin M, Bovi G, Rabuffetti M et al. Reliability of instrumented movement analysis as outcome measure in Charcot-Marie-Tooth disease: results from a multitask locomotor protocol. Gait and Posture 2011;34:36-43.

Verhoeven K, Claeys K, Zuchner S et al. MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2. Brain 2006;129:2093-102.

Thiam A, Sene Fd, Ndao A, Ndiaye M, Ndiaye I. Charcot-Marie-Tooth disease associated with a pyramidal syndrome: clinical, electrophysiological, and neuropathological study of neuro-muscular biopsies in 14 cases. Dakar Med 2002;47:182-7.

Barhoumi C, Amouri R, Ben Hamida C et al. Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3. Neuromusc Disord 2001;11:27-34.

Barhoumi C, Machghoul S, Hintati F. Identification of a new genetic entity in the form of an autosomal dominant axonal Charcot-Marie-Tooth disease associated with periodic paralyses and pyramidal syndrome. Tun Med 2005;83:547-55.

Manyam N, Cowell H, Katz L. Charcot-Marie-Tooth disease and schizophrenia in identical twins. JAMA 1979;241:54-5.

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Published

2014-01-21

Issue

Section

brief case reports