Sökning: onr:"swepub:oai:lup.lub.lu.se:9e54c712-d4e4-4cfb-889e-f33c41939210" >
Clinical and Molecu...
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant : Elucidating its Role in Collagen VI-related Myopathies
-
- Villar-Quiles, Rocío N. (författare)
- Pitié-Salpêtrière University Hospital,Paris-Sorbonne University
-
- Donkervoort, Sandra (författare)
- National Institute of Neurological Disorders and Stroke (NINDS)
-
- De Becdelièvre, Alix (författare)
- Pitié-Salpêtrière University Hospital,Henri Mondor Hospital
-
visa fler...
-
- Gartioux, Corine (författare)
- Paris-Sorbonne University
-
- Jobic, Valérie (författare)
- Pitié-Salpêtrière University Hospital
-
- Foley, A. Reghan (författare)
- National Institute of Neurological Disorders and Stroke (NINDS)
-
- McCarty, Riley M. (författare)
- National Institute of Neurological Disorders and Stroke (NINDS)
-
- Hu, Ying (författare)
- National Institute of Neurological Disorders and Stroke (NINDS)
-
- Menassa, Rita (författare)
- Lyon Civil Hospital / Hospices Civils de Lyon
-
- Michel, Laurence (författare)
- Lyon Civil Hospital / Hospices Civils de Lyon
-
- Gousse, Gaelle (författare)
- University Hospital Of Saint-Etienne
-
- Lacour, Arnaud (författare)
- University Hospital Of Saint-Etienne
-
- Petiot, Philippe (författare)
- Claude Bernard University Lyon 1
-
- Streichenberger, Nathalie (författare)
- Lyon Civil Hospital / Hospices Civils de Lyon
-
- Choumert, Ariane (författare)
- Centre Hospitalier Universitaire Sud Réunion
-
- Declerck, Leá (författare)
- Centre Hospitalier Universitaire Sud Réunion
-
- Urtizberea, J. A. (författare)
- Hôpital Marin de Hendaye
-
- Sole, Guilhem (författare)
- Groupe Hospitalier Pellegrin
-
- Furby, Alain (författare)
- Hopital Nord CHU de Sainte-Etienne
-
- Cérino, Matthieu (författare)
- La Timone University Hospital
-
- Krahn, Martin (författare)
- La Timone University Hospital
-
- Campana- Salort, Emmanuelle (författare)
- La Timone University Hospital
-
- Ferreiro, Ana (författare)
- Pitié-Salpêtrière University Hospital,Paris Diderot University
-
- Eymard, Bruno (författare)
- Pitié-Salpêtrière University Hospital
-
- Bönnemann, Carsten G. (författare)
- National Institute of Neurological Disorders and Stroke (NINDS)
-
- Bharucha-Goebel, Diana (författare)
- National Institute of Neurological Disorders and Stroke (NINDS),Children’s National Health System, Washington
-
- Sumner, Charlotte J. (författare)
- Johns Hopkins University School of Medicine
-
- Connolly, Anne M. (författare)
- Ohio State University
-
- Richard, Pascale (författare)
- Pitié-Salpêtrière University Hospital
-
- Allamand, Valérie (författare)
- Lund University,Lunds universitet,Muskelbiologi,Forskargrupper vid Lunds universitet,Muscle Biology,Lund University Research Groups,Paris-Sorbonne University
-
- Métay, Corinne (författare)
- Pitié-Salpêtrière University Hospital,Paris-Sorbonne University
-
- Stojkovic, Tanya (författare)
- Paris-Sorbonne University,Pitié-Salpêtrière University Hospital
-
visa färre...
-
(creator_code:org_t)
- 2021
- 2021
- Engelska 13 s.
-
Ingår i: Journal of Neuromuscular Diseases. - 2214-3599. ; 8:4, s. 633-645
- Relaterad länk:
-
http://dx.doi.org/10...
-
visa fler...
-
https://lup.lub.lu.s...
-
https://doi.org/10.3...
-
visa färre...
Abstract
Ämnesord
Stäng
- Background: Dominant and recessive autosomal pathogenic variants in the three major genes (COL6A1-A2-A3) encoding the extracellular matrix protein collagen VI underlie a group of myopathies ranging from early-onset severe conditions (Ullrich congenital muscular dystrophy) to milder forms maintaining independent ambulation (Bethlem myopathy). Diagnosis is based on the combination of clinical presentation, muscle MRI, muscle biopsy, analysis of collagen VI secretion, and COL6A1-A2-A3 genetic analysis, the interpretation of which can be challenging. Objective: To refine the phenotypical spectrum associated with the frequent COL6A3 missense variant c.7447A>G (p.Lys2483Glu). Methods: We report the clinical and molecular findings in 16 patients: 12 patients carrying this variant in compound heterozygosity with another COL6A3 variant, and four homozygous patients. Results: Patients carrying this variant in compound heterozygosity with a truncating COL6A3 variant exhibit a phenotype consistent with COL6-related myopathies (COL6-RM), with joint contractures, proximal weakness and skin abnormalities. All remain ambulant in adulthood and only three have mild respiratory involvement. Most show typical muscle MRI findings. In five patients, reduced collagen VI secretion was observed in skin fibroblasts cultures. All tested parents were unaffected heterozygous carriers. Conversely, two out of four homozygous patients did not present with the classical COL6-RM clinical and imaging findings. Collagen VI immunolabelling on cultured fibroblasts revealed rather normal secretion in one and reduced secretion in another. Muscle biopsy from one homozygous patient showed myofibrillar disorganization and rimmed vacuoles. Conclusions: In light of our results, we postulate that the COL6A3 variant c.7447A>G may act as a modulator of the clinical phenotype. Thus, in patients with a typical COL6-RM phenotype, a second variant must be thoroughly searched for, while for patients with atypical phenotypes further investigations should be conducted to exclude alternative causes. This works expands the clinical and molecular spectrum of COLVI-related myopathies.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Neurologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Neurology (hsv//eng)
Nyckelord
- COL6A3
- collagen type VI
- Collagen VI-related myopathies
- congenital muscular dystrophy (CMD)
- limb-girdle muscular dystrophy (LGMD)
- muscular MRI
- neuromuscular disorders
- NGS
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
Hitta via bibliotek
Till lärosätets databas
- Av författaren/redakt...
-
Villar-Quiles, R ...
-
Donkervoort, San ...
-
De Becdelièvre, ...
-
Gartioux, Corine
-
Jobic, Valérie
-
Foley, A. Reghan
-
visa fler...
-
McCarty, Riley M ...
-
Hu, Ying
-
Menassa, Rita
-
Michel, Laurence
-
Gousse, Gaelle
-
Lacour, Arnaud
-
Petiot, Philippe
-
Streichenberger, ...
-
Choumert, Ariane
-
Declerck, Leá
-
Urtizberea, J. A ...
-
Sole, Guilhem
-
Furby, Alain
-
Cérino, Matthieu
-
Krahn, Martin
-
Campana- Salort, ...
-
Ferreiro, Ana
-
Eymard, Bruno
-
Bönnemann, Carst ...
-
Bharucha-Goebel, ...
-
Sumner, Charlott ...
-
Connolly, Anne M ...
-
Richard, Pascale
-
Allamand, Valéri ...
-
Métay, Corinne
-
Stojkovic, Tanya
-
visa färre...
- Om ämnet
-
- MEDICIN OCH HÄLSOVETENSKAP
-
MEDICIN OCH HÄLS ...
-
och Medicinska och f ...
-
och Medicinsk geneti ...
-
- MEDICIN OCH HÄLSOVETENSKAP
-
MEDICIN OCH HÄLS ...
-
och Klinisk medicin
-
och Neurologi
- Artiklar i publikationen
-
Journal of Neuro ...
- Av lärosätet
-
Lunds universitet