<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Abbott L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Prior to the introduction of disease-modifying treatments (DMTs), children with type 1 spinal muscular atrophy (SMA) typically did not survive beyond the age of 2 years; management was mainly palliative. Novel therapies have made this a treatable condition, resulting in increased life expectancy and more time spent upright. Survival and improved function mean spinal asymmetry is a new complication with limited data on its prevalence and severity and no current guidelines on management and treatment. This study aimed to evaluate the spinal presentation and management of type 1 SMA children on nusinersen across the SMA-REACH UK network.&lt;h4>Methods&lt;/h4>Spinal presentation and management of 80 children (age range 4 months-14 years, median 4 years 2 months) with type 1 SMA on</pubmed_abstract><journal>BMJ open</journal><pagination>e082240</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11784377</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Spinal presentations in children with type 1 spinal muscular atrophy on nusinersen treatment across the SMA-REACH UK network: a retrospective national observational study.</pubmed_title><pmcid>PMC11784377</pmcid><pubmed_authors>Scoto M</pubmed_authors><pubmed_authors>White K</pubmed_authors><pubmed_authors>Emery N</pubmed_authors><pubmed_authors>D'Urso S</pubmed_authors><pubmed_authors>Milev E</pubmed_authors><pubmed_authors>Pallant L</pubmed_authors><pubmed_authors>Mason F</pubmed_authors><pubmed_authors>Sheehan J</pubmed_authors><pubmed_authors>McMurchie H</pubmed_authors><pubmed_authors>Longatto J</pubmed_authors><pubmed_authors>Rohwer A</pubmed_authors><pubmed_authors>Munot P</pubmed_authors><pubmed_authors>Raab R</pubmed_authors><pubmed_authors>NicFhirleinn G</pubmed_authors><pubmed_authors>SMA-REACH UK Network Physiotherapists</pubmed_authors><pubmed_authors>Gregson S</pubmed_authors><pubmed_authors>Selby V</pubmed_authors><pubmed_authors>Wolfe A</pubmed_authors><pubmed_authors>Topping A</pubmed_authors><pubmed_authors>Manzur A</pubmed_authors><pubmed_authors>Panagiotopoulou E</pubmed_authors><pubmed_authors>Abbott L</pubmed_authors><pubmed_authors>Main M</pubmed_authors><pubmed_authors>Muntoni F</pubmed_authors><pubmed_authors>Baranello G</pubmed_authors><pubmed_authors>Wadsworth S</pubmed_authors><pubmed_authors>Moustoukas J</pubmed_authors><pubmed_authors>Vann F</pubmed_authors><pubmed_authors>Rye C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spinal presentations in children with type 1 spinal muscular atrophy on nusinersen treatment across the SMA-REACH UK network: a retrospective national observational study.</name><description>&lt;h4>Background&lt;/h4>Prior to the introduction of disease-modifying treatments (DMTs), children with type 1 spinal muscular atrophy (SMA) typically did not survive beyond the age of 2 years; management was mainly palliative. Novel therapies have made this a treatable condition, resulting in increased life expectancy and more time spent upright. Survival and improved function mean spinal asymmetry is a new complication with limited data on its prevalence and severity and no current guidelines on management and treatment. This study aimed to evaluate the spinal presentation and management of type 1 SMA children on nusinersen across the SMA-REACH UK network.&lt;h4>Methods&lt;/h4>Spinal presentation and management of 80 children (age range 4 months-14 years, median 4 years 2 months) with type 1 SMA on</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-06-06T23:42:05.76Z</modification><creation>2026-06-06T03:11:10.047Z</creation></dates><accession>S-EPMC11784377</accession><cross_references><pubmed>39842910</pubmed><doi>10.1136/bmjopen-2023-082240</doi></cross_references></HashMap>