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DOI: 10.1590/0004-282X20190008
Unilateral abdominal protrusion as the main diagnostic sign of facioscapulohumeral dystrophy
Protrusão abdominal unilateral como principal sinal diagnóstico de distrofia fáscio-escápulo-umeralAuthors
A 48-year-old man presented with slowly progressive right arm weakness and cervical pain over the last 20 years. Previous electromyography/nerve conduction studies showed a neurogenic pattern on the right cervical myotomes and he received the diagnosis of focal motor neuron disease. No relevant family history was identified. On our initial evaluation, an asymmetrical abdominal protrusion was noted as well as a mild right arm weakness and atrophy ([Figure]), leading to the suspicion of facioscapulohumeral dystrophy (FSHD). A DNA test detected a D4Z4 repeat contraction on chromosome 4qA, confirming the diagnosis. The frequency of an asymmetrical protuberant abdomen in these patients is not known. Although more than 80% of FSHD patients have affected abdominal muscles and 78% have some degree of asymmetry shown in MRI evaluation, less than 3% present with asymmetrical abdominal muscle involvement[1]. Even though it is an uncommon sign, the association of abdominal weakness and asymmetry is a key feature to consider FSHD diagnosis, especially in milder forms[2].


Conflict of interest:
There is no conflict of interest to declare.
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References
- 1 Tasca G, Monforte M, Ottaviani P, Pelliccioni M, Frusciante R, Laschena F et al. Magnetic resonance imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: Pattern refinement and implications for clinical trials. Ann Neurol. 2016;79(5):854-64. https://doi.org/10.1002/ana.24640
- 2 Mul K, Lassche S, Voermans NC, Padberg GW, Horlings CG, Engelen BG. What's in a name? The clinical features of facioscapulohumeral muscular dystrophy. Pract Neurol. 2016;16(3):201-7. https://doi.org/10.1136/practneurol-2015-001353
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Publication History
Received: 05 October 2018
Accepted: 08 November 2018
Article published online:
21 August 2023
© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Tasca G, Monforte M, Ottaviani P, Pelliccioni M, Frusciante R, Laschena F et al. Magnetic resonance imaging in a large cohort of facioscapulohumeral muscular dystrophy patients: Pattern refinement and implications for clinical trials. Ann Neurol. 2016;79(5):854-64. https://doi.org/10.1002/ana.24640
- 2 Mul K, Lassche S, Voermans NC, Padberg GW, Horlings CG, Engelen BG. What's in a name? The clinical features of facioscapulohumeral muscular dystrophy. Pract Neurol. 2016;16(3):201-7. https://doi.org/10.1136/practneurol-2015-001353


