spinal muscular atrophynational newborn screening programmegovernment
…A national newborn screening programme for spinal muscular atrophy (SMA) will be rolled out throughout England, the government has…
9articles mentioning diseases
9disease mentions
1distinct diseases extracted
0%of mentions human-reviewed
Active filtersEntity: Spinal muscular atrophy ×
Spinal muscular atrophy
This disease is selected. Its supporting articles are shown below.
Articles mentioning Spinal muscular atrophy
9 articles · page 1 of 1Spinal muscular atrophySMA type 3nusinersen
…Spinal muscular atrophy (SMA) is a neuromuscular disorder caused by SMN1 gene mutations…
spinal muscular atrophynusinersenonasemnogene abeparvovecadeno-associated virus-based gene replacement therapynewborn screening
…A 10-month-old girl with genetically confirmed spinal muscular atrophy (SMA) (homozygous deletion of SMN1 exon 7) was identified throu…
89.5%
Spinal muscular atrophySMA
…Introduction 5q Spinal muscular atrophy (SMA) causes progressive, muscle weakness affecting the limbs, …
Spinal muscular atrophySMARisdiplamSt George’sSalfordSheffielddisease modifying therapy
…Background Spinal muscular atrophy (SMA) is a genetic neuromuscular disorder caused by mutations i…
SMA3spinal muscular atrophySMA2SMA1SMAcholecalciferolNational Hospital for Neurology and Neurosurgerydisease-modifying treatments
…ology and Neurosurgery from 2022-2025.Results SMA subtypes were SMA3 (55%), SMA2 (44%) and SMA1 (1%).Fracture incidence was 23%, of …
92.0%
Spinal Muscular AtrophySMA2SMA1SMA3SMA4SMARisdiplamNusinersenNational Hospital for Neurology and NeurosurgeryNHNN
…und methodology We present the UK’s largest single-centre adult Spinal Muscular Atrophy (SMA) cohort. Data was prospectively recorded at the National H…
spinal muscular atrophycurative therapyUK Generation Study
…onable diagnosis is made for around every 200 babies, including spinal muscular atrophy detected before symptom onset, enabling curative therapy.2…
cystic fibrosisfamilial dysautonomiaCanavan diseasefragile X syndromeTay-Sachs diseasespinal muscular atrophyhaemoglobinopathiesfounder mutationsCanadian College of Medical GeneticistsCCMG
…ons, based on Canadian experience with ethnicity-based testing: cystic fibrosis, fragile X syndrome, spinal muscular atrophy, haemoglobinopathi…