Literature DB >> 32515646

Clinical Course in a Patient With Spinal Muscular Atrophy Type 0 Treated With Nusinersen and Onasemnogene Abeparvovec.

Susan E Matesanz1, Candace Curry2, Brianna Gross1, Adam I Rubin3,4, Rebecca Linn3,5, Sabrina W Yum1,6, Elizabeth A Kichula1,6.   

Abstract

Spinal muscular atrophy type 0 is the most severe phenotype of the disease, with patients presenting with contractures, weakness, and respiratory failure at birth, and is typically fatal within weeks. We describe the case of a patient with spinal muscular atrophy type 0 who was treated with both nusinersen and onasemnogene abeparvovec. She has made modest motor improvements since treatment initiation with a 30-point improvement in CHOP-INTEND score, and continues to make motor gains at age 13 months without regression of function, although she remains profoundly weak. Although she has had motor improvements, she has also had continued systemic complications from her spinal muscular atrophy, including chronic respiratory failure, dysphagia, congenital heart malformation, digit necrosis, and diffuse macular rash. This case highlights the challenges in treating those with more severe disease phenotypes and raises questions of how some systemic complications may respond to current SMN replacement therapies.

Entities:  

Keywords:  ethics; infant; neuropathy; outcome; treatment

Year:  2020        PMID: 32515646     DOI: 10.1177/0883073820928784

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  8 in total

Review 1.  Spinal muscular atrophy.

Authors:  Eugenio Mercuri; Charlotte J Sumner; Francesco Muntoni; Basil T Darras; Richard S Finkel
Journal:  Nat Rev Dis Primers       Date:  2022-08-04       Impact factor: 65.038

Review 2.  Restoring Protein Expression in Neuromuscular Conditions: A Review Assessing the Current State of Exon Skipping/Inclusion and Gene Therapies for Duchenne Muscular Dystrophy and Spinal Muscular Atrophy.

Authors:  Omar Sheikh; Toshifumi Yokota
Journal:  BioDrugs       Date:  2021-06-07       Impact factor: 5.807

Review 3.  [Scoliosis in spinal muscular atrophy].

Authors:  T-L Vu-Han; M J Reisener; M Putzier; M Pumberger
Journal:  Orthopade       Date:  2021-07-07       Impact factor: 1.087

4.  Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy.

Authors:  Yu Xia; Yijie Feng; Lu Xu; Xiaoyang Chen; Feng Gao; Shanshan Mao
Journal:  Front Genet       Date:  2021-03-10       Impact factor: 4.599

Review 5.  Restoring SMN Expression: An Overview of the Therapeutic Developments for the Treatment of Spinal Muscular Atrophy.

Authors:  Tejal Aslesh; Toshifumi Yokota
Journal:  Cells       Date:  2022-01-26       Impact factor: 6.600

Review 6.  Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies.

Authors:  Panagiota Panagiotou; Christina Kanaka-Gantenbein; Athanasios G Kaditis
Journal:  Children (Basel)       Date:  2022-08-11

Review 7.  Dysphagia Phenotypes in Spinal Muscular Atrophy: The Past, Present, and Promise for the Future.

Authors:  Katlyn Elizabeth McGrattan; Robert J Graham; Christine J DiDonato; Basil T Darras
Journal:  Am J Speech Lang Pathol       Date:  2021-04-06       Impact factor: 2.408

8.  Nusinersen in type 0 spinal muscular atrophy: should we treat?

Authors:  Eloisa Tiberi; Simonetta Costa; Marika Pane; Francesca Priolo; Roberto de Sanctis; Domenico Romeo; Francesco D Tiziano; Giorgio Conti; Giovanni Vento; Eugenio Mercuri
Journal:  Ann Clin Transl Neurol       Date:  2020-11-04       Impact factor: 5.430

  8 in total

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