Skip to main content

Advertisement

Log in

MRI findings, patterns of disease distribution, and muscle fat fraction calculation in five patients with Charcot-Marie-Tooth type 2 F disease

  • Scientific Article
  • Published:
Skeletal Radiology Aims and scope Submit manuscript

Abstract

Purpose

To describe the magnetic resonance imaging (MRI) pattern of muscle involvement and disease progression in five patients with late-onset Charcot-Marie-Tooth (CMT) disease type 2 F, due to a previously unknown mutation.

Materials and methods

Five patients (three males, two females) underwent MRI of the lower limbs to define the pattern of muscle involvement and evaluate the muscle fat fraction (MFF) of residual thigh muscle with gradient-echo (GRE) dual-echo dual-flip angle technique. Evaluation of fatty infiltration both by visual inspection and MFF calculation was performed.

Results

A proximal-to-distal gradient of muscle involvement was depicted in male patients with extensive muscle wasting of lower legs, less severe impairment of distal thigh muscles, and sparing of proximal thigh muscles. A peculiar phenotype finding was that no or only slight muscle abnormalities could be found in the two female patients.

Conclusion

We described the pattern of muscle involvement and disease progression in a family with CMT disease type 2 F. GRE dual-echo dual-flip angle MRI technique is a valuable technique to obtain a rapid quantification of MFF.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

References

  1. Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth’s disease. Clin Genet. 1974;6:98–118.

    Article  PubMed  CAS  Google Scholar 

  2. Harding AE, Thomas PK. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain. 1980;103:259–80.

    Article  PubMed  CAS  Google Scholar 

  3. Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nat Rev Neurosci. 2003;4:714–26.

    Article  PubMed  CAS  Google Scholar 

  4. Tang B, Liu X, Zhao G, et al. Mutation analysis of the small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease. Arch Neurol. 2005;62:1201–7.

    Article  PubMed  Google Scholar 

  5. Ismailov SM, Fedotov VP, Dadali EL, et al. A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21. Eur J Hum Genet. 2001;9:646–50.

    Article  PubMed  CAS  Google Scholar 

  6. Evgrafov OV, Mersiyanova I, Irobi J, et al. Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nat Genet. 2004;36:602–6.

    Article  PubMed  CAS  Google Scholar 

  7. Houlden H, Laura M, Wavrant-De Vrièze F, Blake J, Wood N, Reilly MM. Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2. Neurology. 2008;71:1656–7.

    Article  Google Scholar 

  8. Gallardo E, Clayes KG, Nelis E, et al. Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation. J Neurol. 2008;255:986–92.

    Article  PubMed  CAS  Google Scholar 

  9. Chung KW, Suh BC, Shy ME, et al. Different clinical and magnetic resonance imaging features between Charcot-Marie-Tooth disease type 1A and 2A. Neuromuscul Disord. 2008;18:610–8.

    Article  PubMed  CAS  Google Scholar 

  10. Gallardo E, Garcia A, Ramon A, et al. Charcot-Marie-Tooth disease type 2J with MPZ Thr124Met mutation: clinico-electrophysiological and MRI study of a family. J Neurol. 2009;256:2061–71.

    Article  PubMed  Google Scholar 

  11. Stillwell G, Kilcoyne RF, Sherman JL. Patterns of muscle atrophy in the lower limbs in patients with Charcot-Marie–-Tooth disease as measured by magnetic resonance imaging. J Foot Ankle Surg. 1995;34:583–6.

    Article  Google Scholar 

  12. Berciano J, Gallardo E, Garcia A, Infante J, Mateo I, Combarros O. Charcot-Marie-Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long-term follow-up study. J Neurol Neurosurg Psychiatry. 2006;77:1169–76.

    Article  PubMed  CAS  Google Scholar 

  13. Gallardo E, Garcıa A, Combarros O, Berciano J. Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles. Brain. 2006;129:426–37.

    Article  PubMed  Google Scholar 

  14. Fabrizi GM, Ferrarini M, Cavallaro T, et al. Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. Neurology. 2007;69:291–5.

    Article  PubMed  CAS  Google Scholar 

  15. Chung KW, Kim SB, Park KD, et al. Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations. Brain. 2006;129:2103–18.

    Article  PubMed  CAS  Google Scholar 

  16. Goutallier D, Postel JM, Bernageau J, Lavau L, Voisin MC. Fatty muscle degeneration in cuff ruptures. Pre- and postoperative evaluation by CT scan. Clin Orthop Relat Res. 1994;304:78–83.

    PubMed  Google Scholar 

  17. Price AE, Maisel R, Drennan JC. Computed tomography analysis of pes cavum. J Pediatr Orthop. 1993;13:646–53.

    PubMed  CAS  Google Scholar 

  18. Gaeta M, Scribano E, Mileto A et al. Muscle fat fraction in neuromuscular disorders: dual-echo dual-flip-angle spoiled gradient-recalled MR imaging technique for quantification-a feasibility study. Radiology 2011;259:487–94. doi:10.1148/radiol.10101108.

    Google Scholar 

  19. May DA, Disler DG, Jones EA, Balkissoon AA, Manaster BJ. Abnormal signal intensity in skeletal muscle at MRI: patterns, pearls, and pitfalls. Radiographics. 2000;20:S295–315.

    PubMed  Google Scholar 

  20. Mercuri E, Jungbluth H, Muntoni F. Muscle imaging in clinical practice: diagnostic value of muscle magnetic resonance imaging in inherited neuromuscular disorders. Curr Opin Neurol. 2005;18:526–37.

    Article  PubMed  Google Scholar 

  21. Martini R, Berciano J, Van Broeckhoven C. 5th Workshop of the European CMT Consortium: therapeutic approachs in CMT neuropathies and related disorders, 23–25 April 1999, Soestduinen, The Netherlands. Neuromuscul Disord. 2000;10:69–74.

    Article  PubMed  CAS  Google Scholar 

  22. Degardin A, Morillon D, Lacour A, Cotten A, Vermersch P, Stojkovic T. Morphologic imaging in muscular dystrophies and inflammatory myopathies. Skeletal Radiol. 2010;39:1219–27.

    Article  PubMed  Google Scholar 

  23. Wattjes MP, Kley RA, Fischer D. Neuromuscular imaging in inherited muscle diseases. Eur Radiol. 2010;20:2447–60.

    Article  PubMed  Google Scholar 

  24. Scott OM, Hyde SA, Goddard C, Dubowitz V. Quantitation of muscle function in children: a prospective study in Duchenne muscular dystrophy. Muscle Nerve. 1982;5:291–301.

    Article  PubMed  CAS  Google Scholar 

  25. Bruhn H, Frahm J, Gyngell ML, Merbodt KD, Haenicke W, Sauter R. Localized proton NMR spectroscopy using stimulated echoes: application to human skeletal muscle in vivo. Magn Reson Med. 1991;17:82–94.

    Article  PubMed  CAS  Google Scholar 

  26. Wren TAL, Bluml S, Tseng-Ong L, Gilsanz V. Three-point technique of fat quantification of muscle tissue as a marker of disease progression in Duchenne muscular dystrophy: preliminary study. AJR Am J Roentgenol. 2008;190:W8–12.

    Article  PubMed  Google Scholar 

  27. Gaeta M, Minutoli F, Toscano A, et al. Opposed-phase MR imaging of lipid storage myopathy in a case of Chanarin-Dorfman disease. Skeletal Radiol. 2008;37:1053–7.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Achille Mileto.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gaeta, M., Mileto, A., Mazzeo, A. et al. MRI findings, patterns of disease distribution, and muscle fat fraction calculation in five patients with Charcot-Marie-Tooth type 2 F disease. Skeletal Radiol 41, 515–524 (2012). https://doi.org/10.1007/s00256-011-1199-y

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00256-011-1199-y

Keywords

Navigation