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

Eloisa Tiberi, Simonetta Costa, Marika Pane, Francesca Priolo, Roberto De Sanctis, Domenico M. Romeo, Francesco Danilo Tiziano, Giorgio Conti, Giovanni Vento, Eugenio Mercuri

2020Annals of Clinical and Translational Neurology23 citationsDOIOpen Access PDF

Abstract

A male infant affected by type 0 SMA with one copy of SMN2 received early treatment with Nusinersen at the age of 13 days. He showed mild motor improvement 2 months after treatment started but despite also showing some minimal respiratory improvement, required tracheostomy at the age of 4 months and had increasing cardiac and autonomic dysfunction leading to exitus at 5 months. Our findings, expanding the results available on Nusinersen, confirm its relative efficacy in the most severely affected infants and provide clinical evidence to be used at the time requests for treating severe infants are discussed.

Topics & Concepts

MedicineSpinal muscular atrophyAtrophyPhysical medicine and rehabilitationBioinformaticsPathologyDiseaseBiologyNeurogenetic and Muscular Disorders ResearchRNA modifications and cancerCongenital Anomalies and Fetal Surgery
Nusinersen in type 0 spinal muscular atrophy: should we treat? | Litcius