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1655 news items
Research
Loss of function of JPH1, which encodes junctophilin, causes congenital myopathy
On 05/11/2024
Four individuals from unrelated consanguineous families, two of European origin, one of Khmer origin and one of Middle Eastern origin all presented with congenital myopathy…
Research
Riboflavin transporter deficiency: the importance of treating early, even if it doesn’t solve everything
On 04/11/2024
A retrospective study describes a population of 11 children with riboflavin transporter deficiency (RTD) type 2, all carriers of mutations in the SLC52A2 gene, followed…
Research
Cerebral abnormalities in dysferlinopathies?
On 31/10/2024
Slovakian and Austrian clinicians report the case of a family in which dysferlin deficiency was identified at the same time as structural and functional cerebral…
Research
Towards a new therapeutic approach to cardiovascular complications in progeria?
On 30/10/2024
Hutchinson-Gilford syndrome (HGPS or progeria) is an autosomal dominant disease caused by a mutation in the LMNA gene, coding for type A lamins, which results…
Research
Thrombotic microangiopathy: a formidable complication of gene therapy
On 30/10/2024
A multidisciplinary group of international experts has examined one of the complications that can arise during systemic gene therapy protocols, particularly in children with spinal…
Research
A multi-factorial approach to urinary disorders in DMD
On 29/10/2024
Turkish physiotherapists report on their experience in assessing symptoms, disorders and signs of the lower urinary tract in children with Duchenne muscular dystrophy (DMD): 45…
Research
Clinical and biological markers to differentiate between ocular and generalised forms of myasthenia gravis
On 28/10/2024
Danish clinicians reviewed 350 records of patients with ocular or generalised forms of autoimmune myasthenia : clinical, electrophysiological and serological data were compiled and compared,…
Research
Towards a better assessment of complex cases of titinopathy
On 28/10/2024
The large size of the TTN gene encoding titin and the existence of numerous isoforms make it difficult to interpret genomic variants. An international consortium…
Research
Belgian family confirms possible link between HLA-DRB1*11:01 and statin-induced myositis
On 25/10/2024
In Belgium, a father and daughter : developed autoimmune necrotising myopathy with HMGCR autoantibodies a few years apart, following treatment with statins; are both carriers…
Research
Beware of phytotherapies in dermatomyositis
On 24/10/2024
American clinicians have studied the prevalence and risk-taking among patients suffering from cutaneous autoimmune diseases who use herbal treatments: These included dermatomyositis and systemic lupus…
Research
Positive feedback on multidisciplinary management of interstitial lung disease in France
On 23/10/2024
Patients with certain inflammatory myopathies are at risk of developing severe interstitial lung disease. French clinicians working in the FAI2R and RespiFil healthcare networks report…
Research
Ventilatory weaning and myasthenic crisis: the experience of Raymond Poincaré University Hospital
On 22/10/2024
Clinicians in the western Ile-de-France region have retrospectively analyzed the clinical and paraclinical data of 126 myasthenia gravis patients who presented with a first myasthenic…
Research
Study of a Russian cohort adds to the phenotypic description of MATR3-linked distal myopathy
On 22/10/2024
Matrin-3 deficiency can give rise to a form of amyotrophic lateral sclerosis (ALS) or distal myopathy with vocal cord paralysis (VCPDM). Russian clinicians report the…
Research
Common in South India, GNE myopathy is associated with a founder effect
On 21/10/2024
Clinicians in southern India, working with other international research teams, have compiled clinical, biological and genetic data from a very large cohort of adult patients…
Research
Granulomatous myositis: a rare form of inflammatory myopathy
On 21/10/2024
French researchers report the clinical and histological data and immunological profile of 26 patients diagnosed with granulomatous myositis: the age of onset was generally very…
Events
‘Fête de la science 2024’ at the Institute
On 18/10/2024
This year, the Fête de la Science was held nationwide from 4 to 12 October 2024. The Institute of Myology opened its doors to the…
Research
L-carnitine and creatine show therapeutic potential in animal models of laminopathy
On 18/10/2024
Amino acid derivatives have been shown to be beneficial in a number of myopathies, including collagenopathies and congenital myopathies. Taiwanese researchers have explored the therapeutic…
Research
A new mouse model of Becker muscular dystrophy
On 18/10/2024
Canadian researchers have developed a new mouse model partially deleted for the gene encoding dystrophin (DMD gene) with the aim of imitating Becker muscular dystrophy:…
Research
Comparative data on vamorolone and prednisone for adrenal suppression
On 16/10/2024
Long-term corticosteroid therapy remains the reference treatment for Duchenne muscular dystrophy (DMD), but is associated with numerous side-effects, including resting of the hypothalamo adrenal axis.…
Research
New data on FOP flare-ups and the efficacy of garetosmab
On 16/10/2024
According to a post-hoc analysis of the results of the Lumina-1 phase II trial of garetosmab versus placebo in fibrodysplasia ossificans progressiva (FOP) : almost…