Novel DES mutation presenting with isolated restrictive respiratory failure. Expanding the clinical spectrum


Por: Alonso-Pérez, J, Barrachina-Esteve, O, Gonzaález-Quereda, L, Viguera-Martinez, ML, Lujaán-Torné, M, Guitart-Feliubadaló, M, Martínez, JM, Carbayo, A, Gallano, P, Díaz-Manera, J, Olivé, M, Rojas-Garcia, R

Publicada: 1 jun 2025 Ahead of Print: 1 jun 2025
Resumen:
Background: Desminopathies are a clinically heterogeneous group of myopathies, with common histological findings in muscle biopsy. Clinically, they usually present with distal and/or proximal muscle weakness often associated with cardiomyopathy. We present 8 patients from 3 unrelated families manifesting isolated respiratory insufficiency without skeletal muscle weakness or heart disease, because of a mutation in the DES gene. Methods: Clinical and demographic data were acquired from medical records. Muscle MRI studies were performed in 6 patients. A muscle biopsy study was performed in the index case from each family. Results: Isolated restrictive respiratory dysfunction was observed in all symptomatic patients, with 2 requiring non-invasive ventilation. Three patients were asymptomatic at the time of the study. None of the patients presented skeletal muscle weakness or heart disease, even after 20 years of disease progression. Muscle MRI showed a common pattern with predominant involvement of the semitendinosus muscle. Muscle biopsy showed patches of cytoplasmic inclusions corresponding to desmin aggregates. The genetic study showed heterozygous presence of the p.Arg415Trp mutation in the DES gene in all patients. Conclusions: We present 5 patients carrying a p.Arg415Trp mutation in the DES gene, manifesting as isolated restrictive respiratory insufficiency without associated skeletal muscle weakness or heart disease. These cases represent a new phenotype associated with DES mutations, thus suggesting that desminopathy should be considered in the diagnostic workup of patients presenting isolated respiratory failure. (c) 2024 Sociedad Espanola de Neurolog & imath;a. Published by Elsevier Espana, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).

Filiaciones:
Alonso-Pérez, J:
 Hosp Univ Nuestra Senora Candelaria, Dept Neurol, Neuromuscular Dis Unit, Tenerife, Spain

 Univ Autonoma Barcelona, Hosp Santa Creu I St Pau, Inst Invest Biomed St Pau IIB St Pau, Dept Neurol,Neuromuscular Dis Unit,Dept Med, Barcelona, Spain

 Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain

Barrachina-Esteve, O:
 Univ Autonoma Barcelona, Parc Tauli Hosp Univ, Inst Invest Innovacio Parc Tauli i I3PT, Dept Neurol, Sabadell, Spain

Gonzaález-Quereda, L:
 Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain

Viguera-Martinez, ML:
 Univ Autonoma Barcelona, Parc Tauli Hosp Univ, Inst Invest Innovacio Parc Tauli i I3PT, Dept Neurol, Sabadell, Spain

Lujaán-Torné, M:
 Univ Autonoma Barcelona, Parc Tauli Hosp Univ, Inst Invest Innovacio Parc Tauli i I3PT, Dept Pulmonol, Sabadell, Spain

Martínez, JM:
 Univ Autonoma Barcelona, Parc Tauli Hosp Univ, Inst Invest Innovacio Parc Tauli i I3PT, Dept Neurol, Sabadell, Spain

Carbayo, A:
 Univ Autonoma Barcelona, Hosp Santa Creu I St Pau, Inst Invest Biomed St Pau IIB St Pau, Dept Neurol,Neuromuscular Dis Unit,Dept Med, Barcelona, Spain

Gallano, P:
 Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain

 Univ Autonoma Barcelona, Hosp Santa Creu I St Pau, Inst Invest Biomed St Pau IIB St Pau, Genet Dept, Barcelona, Spain

Díaz-Manera, J:
 Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain

 Univ Autonoma Barcelona, Parc Tauli Hosp Univ, Inst Invest Innovacio Parc Tauli i I3PT, Genet Dept, Sabadell, Spain

 Newcastle Univ, John Walton Muscular Dystrophy Res Ctr, Newcastle Upon Tyne, England

 Newcastle Hosp NHS Fdn Trust, Newcastle Upon Tyne, England

Olivé, M:
 Univ Autonoma Barcelona, Hosp Santa Creu I St Pau, Inst Invest Biomed St Pau IIB St Pau, Dept Neurol,Neuromuscular Dis Unit,Dept Med, Barcelona, Spain

 Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain

Rojas-Garcia, R:
 Univ Autonoma Barcelona, Hosp Santa Creu I St Pau, Inst Invest Biomed St Pau IIB St Pau, Dept Neurol,Neuromuscular Dis Unit,Dept Med, Barcelona, Spain

 Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain
ISSN: 02134853





NEUROLOGIA
Editorial
ELSEVIER ESPANA SLU, AV JOSEP TARRADELLAS, 20-30, 1ERA PLANTA, BARCELONA, CP-08029, SPAIN, España
Tipo de documento: Article
Volumen: 40 Número: 5
Páginas: 433-441
WOS Id: 001508671900003
ID de PubMed: 40523712
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