Mutations in myelin protein zero (MPZ) are associated with heterogeneous manifestations. In this study, we report clinical, electrophysiological, pathological, and muscle MRI findings from two relatives with MPZ Thr124Met variants, disclosing different phenotypes. The proband was a 73-year-old female with a 12-year-story of atrophy, weakness, and fasciculations in her proximal and distal lower limbs. EMG examination showed neurogenic signs with active denervation together with reduced sensory action potentials, without sensory symptoms. The initial diagnosis was of a slowly progressive lower motor neuron disease (MND) with subclinical sensory axonal neuropathy. Two years later, the observation of her 60-year-old nephew, who had a distal sensory-motor neuropathy, prompted the analysis of inherited neuropathies-related genes and revealed a MPZ Thr124Met mutation in both cases. Our findings expand the clinical spectrum of MPZ-related neuropathy and highlight that Thr124Met mutation may cause a syndrome mimicking MND. The challenging issue to detect sensory features in the diagnostic MND work up is discussed.

Bisogni, G., Romano, A., Conte, A., Tasca, G., Bernardo, D., Luigetti, M., Di Paolantonio, A., Fabrizi, G. M., Patanella, A. K., Meleo, E., Sabatelli, M., Thr124Met myelin protein zero mutation mimicking motor neuron disease, <<AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION>>, 2022; 23 (3-4): 299-304-304. [doi:10.1080/21678421.2021.1946086] [http://hdl.handle.net/10807/204876]

Thr124Met myelin protein zero mutation mimicking motor neuron disease

Tasca G.;Luigetti M.;Di Paolantonio A.;Meleo E.;Sabatelli M.
2021

Abstract

Mutations in myelin protein zero (MPZ) are associated with heterogeneous manifestations. In this study, we report clinical, electrophysiological, pathological, and muscle MRI findings from two relatives with MPZ Thr124Met variants, disclosing different phenotypes. The proband was a 73-year-old female with a 12-year-story of atrophy, weakness, and fasciculations in her proximal and distal lower limbs. EMG examination showed neurogenic signs with active denervation together with reduced sensory action potentials, without sensory symptoms. The initial diagnosis was of a slowly progressive lower motor neuron disease (MND) with subclinical sensory axonal neuropathy. Two years later, the observation of her 60-year-old nephew, who had a distal sensory-motor neuropathy, prompted the analysis of inherited neuropathies-related genes and revealed a MPZ Thr124Met mutation in both cases. Our findings expand the clinical spectrum of MPZ-related neuropathy and highlight that Thr124Met mutation may cause a syndrome mimicking MND. The challenging issue to detect sensory features in the diagnostic MND work up is discussed.
eng
Bisogni, G., Romano, A., Conte, A., Tasca, G., Bernardo, D., Luigetti, M., Di Paolantonio, A., Fabrizi, G. M., Patanella, A. K., Meleo, E., Sabatelli, M., Thr124Met myelin protein zero mutation mimicking motor neuron disease, <>, 2022; 23 (3-4): 299-304-304. [doi:10.1080/21678421.2021.1946086] [http://hdl.handle.net/10807/204876]
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10807/204876
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