Brain MRI abnormalities in a child with spinal muscular atrophy type II

doi:10.1007/s13760-020-01524-x

Case Reports

. 2021 Dec;121(6):1883-1885.

doi: 10.1007/s13760-020-01524-x. Epub 2020 Oct 20.

Brain MRI abnormalities in a child with spinal muscular atrophy type II

Luciana Losito¹, Leonarda Gennaro¹, Elisabetta Lucarelli¹, Antonio Trabacca²

Affiliations

¹ Scientific Institute I.R.C.C.S. "Eugenio Medea", "La Nostra Famiglia", Unit for Severe Disabilities in Developmental Age and Young Adults (Developmental Neurology and Neurorehabilitation), Brindisi Research Centre, Ex Complesso Ospedaliero "A. Di Summa", Piazza "A. Di Summa", 72100, Brindisi, Italy.
² Scientific Institute I.R.C.C.S. "Eugenio Medea", "La Nostra Famiglia", Unit for Severe Disabilities in Developmental Age and Young Adults (Developmental Neurology and Neurorehabilitation), Brindisi Research Centre, Ex Complesso Ospedaliero "A. Di Summa", Piazza "A. Di Summa", 72100, Brindisi, Italy. antonio.trabacca@lanostrafamiglia.it.

PMID: 33079332
DOI: 10.1007/s13760-020-01524-x

Case Reports

Brain MRI abnormalities in a child with spinal muscular atrophy type II

Luciana Losito et al. Acta Neurol Belg. 2021 Dec.

. 2021 Dec;121(6):1883-1885.

doi: 10.1007/s13760-020-01524-x. Epub 2020 Oct 20.

Authors

Luciana Losito¹, Leonarda Gennaro¹, Elisabetta Lucarelli¹, Antonio Trabacca²

Affiliations

¹ Scientific Institute I.R.C.C.S. "Eugenio Medea", "La Nostra Famiglia", Unit for Severe Disabilities in Developmental Age and Young Adults (Developmental Neurology and Neurorehabilitation), Brindisi Research Centre, Ex Complesso Ospedaliero "A. Di Summa", Piazza "A. Di Summa", 72100, Brindisi, Italy.
² Scientific Institute I.R.C.C.S. "Eugenio Medea", "La Nostra Famiglia", Unit for Severe Disabilities in Developmental Age and Young Adults (Developmental Neurology and Neurorehabilitation), Brindisi Research Centre, Ex Complesso Ospedaliero "A. Di Summa", Piazza "A. Di Summa", 72100, Brindisi, Italy. antonio.trabacca@lanostrafamiglia.it.

PMID: 33079332
DOI: 10.1007/s13760-020-01524-x

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References

1. Verhaart IE, Robertson A, Leary R, McMacken G, König K, Kirschner J, Jones CC, Cook SF, Lochmüller H (2017) A multi-source approach to determine SMA incidence and research ready population. J Neurol 264(7):1465–1473 - DOI
1. Trabacca A, Lucarelli E, Pacifico R, Vespino T, Di Liddo A, Losito L (2020) The ICF-CY as a framework for the management of spinal muscular atrophy in the era of gene therapy: a proof-of-concept study. Eur J Phys Rehabil Med 56(2):243–251
1. Lefebvre S, Bürglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M (1995) Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80(1):155–165 - DOI
1. Angelini C, Pinzan E (2019) Advances in imaging of brain abnormalities in neuromuscular disease. Ther Adv Neurol Disord 12:1756286419845567 - PubMed - PMC
1. Polido GJ, Barbosa AF, Morimoto CH, Caromano FA, Favero FM, Zanoteli E, Reed UC, Voos MC (2017) Matching pairs difficulty in children with spinal muscular atrophy type I. Neuromuscul Disord 27(5):419–427 - DOI

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[1] Verhaart IE, Robertson A, Leary R, McMacken G, König K, Kirschner J, Jones CC, Cook SF, Lochmüller H (2017) A multi-source approach to determine SMA incidence and research ready population. J Neurol 264(7):1465–1473 - DOI

[2] Verhaart IE, Robertson A, Leary R, McMacken G, König K, Kirschner J, Jones CC, Cook SF, Lochmüller H (2017) A multi-source approach to determine SMA incidence and research ready population. J Neurol 264(7):1465–1473 - DOI

[3] Trabacca A, Lucarelli E, Pacifico R, Vespino T, Di Liddo A, Losito L (2020) The ICF-CY as a framework for the management of spinal muscular atrophy in the era of gene therapy: a proof-of-concept study. Eur J Phys Rehabil Med 56(2):243–251

[4] Trabacca A, Lucarelli E, Pacifico R, Vespino T, Di Liddo A, Losito L (2020) The ICF-CY as a framework for the management of spinal muscular atrophy in the era of gene therapy: a proof-of-concept study. Eur J Phys Rehabil Med 56(2):243–251

[5] Lefebvre S, Bürglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M (1995) Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80(1):155–165 - DOI

[6] Lefebvre S, Bürglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M (1995) Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80(1):155–165 - DOI

[7] Angelini C, Pinzan E (2019) Advances in imaging of brain abnormalities in neuromuscular disease. Ther Adv Neurol Disord 12:1756286419845567 - PubMed - PMC

[8] Angelini C, Pinzan E (2019) Advances in imaging of brain abnormalities in neuromuscular disease. Ther Adv Neurol Disord 12:1756286419845567 - PubMed - PMC

[9] Polido GJ, Barbosa AF, Morimoto CH, Caromano FA, Favero FM, Zanoteli E, Reed UC, Voos MC (2017) Matching pairs difficulty in children with spinal muscular atrophy type I. Neuromuscul Disord 27(5):419–427 - DOI

[10] Polido GJ, Barbosa AF, Morimoto CH, Caromano FA, Favero FM, Zanoteli E, Reed UC, Voos MC (2017) Matching pairs difficulty in children with spinal muscular atrophy type I. Neuromuscul Disord 27(5):419–427 - DOI

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Brain MRI abnormalities in a child with spinal muscular atrophy type II

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Brain MRI abnormalities in a child with spinal muscular atrophy type II

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