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Developmental milestones in type I spinal muscular atrophy

The aim of this retrospective multicentric study was to assess developmental milestones longitudinally in type I SMA infants using the Hammersmith Infant Neurological Examination. Thirty-three type I SMA infants, who classically do not achieve the ability to sit unsupported, were included in the stu...

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Autores principales: De Sanctis, Roberto, Coratti, Giorgia, Pasternak, Amy, Montes, Jacqueline, Pane, Marika, Mazzone, Elena S., Young, Sally Dunaway, Salazar, Rachel, Quigley, Janet, Pera, Maria C., Antonaci, Laura, Lapenta, Leonardo, Glanzman, Allan M., Tiziano, Danilo, Muntoni, Francesco, Darras, Basil T., De Vivo, Darryl C., Finkel, Richard, Mercuri, Eugenio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091285/
https://www.ncbi.nlm.nih.gov/pubmed/27769560
http://dx.doi.org/10.1016/j.nmd.2016.10.002
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author De Sanctis, Roberto
Coratti, Giorgia
Pasternak, Amy
Montes, Jacqueline
Pane, Marika
Mazzone, Elena S.
Young, Sally Dunaway
Salazar, Rachel
Quigley, Janet
Pera, Maria C.
Antonaci, Laura
Lapenta, Leonardo
Glanzman, Allan M.
Tiziano, Danilo
Muntoni, Francesco
Darras, Basil T.
De Vivo, Darryl C.
Finkel, Richard
Mercuri, Eugenio
author_facet De Sanctis, Roberto
Coratti, Giorgia
Pasternak, Amy
Montes, Jacqueline
Pane, Marika
Mazzone, Elena S.
Young, Sally Dunaway
Salazar, Rachel
Quigley, Janet
Pera, Maria C.
Antonaci, Laura
Lapenta, Leonardo
Glanzman, Allan M.
Tiziano, Danilo
Muntoni, Francesco
Darras, Basil T.
De Vivo, Darryl C.
Finkel, Richard
Mercuri, Eugenio
author_sort De Sanctis, Roberto
collection PubMed
description The aim of this retrospective multicentric study was to assess developmental milestones longitudinally in type I SMA infants using the Hammersmith Infant Neurological Examination. Thirty-three type I SMA infants, who classically do not achieve the ability to sit unsupported, were included in the study. Our results confirmed that all patients had a score of 0 out of a scale of 4 on items assessing sitting, rolling, crawling, standing or walking. A score of more than 0 was only achieved in three items: head control (n = 13), kicking (n = 15) and hand grasp (n = 18). In these items, the maximal score achieved was 1 out of a scale of 4, indicating only partial achievement of the milestone. Infants with symptom onset after 6 months of age had longer preservation of a score of 1 when compared to those with onset before 6 months of age. Our results suggest that even when current standards of care are applied, developmental milestones are rarely even partially achieved as part of natural history in type I SMA infants. No infants in this study achieved a major milestone such as rolling over, or sitting independently, which would therefore represent robust outcomes in future interventional trials.
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spelling pubmed-50912852016-11-07 Developmental milestones in type I spinal muscular atrophy De Sanctis, Roberto Coratti, Giorgia Pasternak, Amy Montes, Jacqueline Pane, Marika Mazzone, Elena S. Young, Sally Dunaway Salazar, Rachel Quigley, Janet Pera, Maria C. Antonaci, Laura Lapenta, Leonardo Glanzman, Allan M. Tiziano, Danilo Muntoni, Francesco Darras, Basil T. De Vivo, Darryl C. Finkel, Richard Mercuri, Eugenio Neuromuscul Disord Article The aim of this retrospective multicentric study was to assess developmental milestones longitudinally in type I SMA infants using the Hammersmith Infant Neurological Examination. Thirty-three type I SMA infants, who classically do not achieve the ability to sit unsupported, were included in the study. Our results confirmed that all patients had a score of 0 out of a scale of 4 on items assessing sitting, rolling, crawling, standing or walking. A score of more than 0 was only achieved in three items: head control (n = 13), kicking (n = 15) and hand grasp (n = 18). In these items, the maximal score achieved was 1 out of a scale of 4, indicating only partial achievement of the milestone. Infants with symptom onset after 6 months of age had longer preservation of a score of 1 when compared to those with onset before 6 months of age. Our results suggest that even when current standards of care are applied, developmental milestones are rarely even partially achieved as part of natural history in type I SMA infants. No infants in this study achieved a major milestone such as rolling over, or sitting independently, which would therefore represent robust outcomes in future interventional trials. Pergamon Press 2016-11 /pmc/articles/PMC5091285/ /pubmed/27769560 http://dx.doi.org/10.1016/j.nmd.2016.10.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
De Sanctis, Roberto
Coratti, Giorgia
Pasternak, Amy
Montes, Jacqueline
Pane, Marika
Mazzone, Elena S.
Young, Sally Dunaway
Salazar, Rachel
Quigley, Janet
Pera, Maria C.
Antonaci, Laura
Lapenta, Leonardo
Glanzman, Allan M.
Tiziano, Danilo
Muntoni, Francesco
Darras, Basil T.
De Vivo, Darryl C.
Finkel, Richard
Mercuri, Eugenio
Developmental milestones in type I spinal muscular atrophy
title Developmental milestones in type I spinal muscular atrophy
title_full Developmental milestones in type I spinal muscular atrophy
title_fullStr Developmental milestones in type I spinal muscular atrophy
title_full_unstemmed Developmental milestones in type I spinal muscular atrophy
title_short Developmental milestones in type I spinal muscular atrophy
title_sort developmental milestones in type i spinal muscular atrophy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5091285/
https://www.ncbi.nlm.nih.gov/pubmed/27769560
http://dx.doi.org/10.1016/j.nmd.2016.10.002
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