Epilepsy, epileptiform discharges and features of brain magnetic resonance imaging in merosin-deficient muscular dystrophy
Background. Merosin-deficient muscular dystrophy (MDMD) is a neuromuscular disease resulting from the emergence of biallelic variants in the LAMA2 gene and manifested by progressive muscle weakness, diffuse hypotonia, impaired posture, contractures of large joints, and respiratory pathology. Epileps...
Saved in:
| Main Authors: | A. V. Monakhova, E. D. Belousova, Z. K. Gorchkhanova |
|---|---|
| Format: | Article |
| Language: | Russian |
| Published: |
IRBIS LLC
2025-07-01
|
| Series: | Эпилепсия и пароксизмальные состояния |
| Subjects: | |
| Online Access: | https://www.epilepsia.su/jour/article/view/1207 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM
by: O. A. Klochkova, et al.
Published: (2014-07-01) -
Distrofia muscular congênita e deficiência de merosina Congenital muscular dystrophy and merosin deficiency
by: Lineu Cesar Werneck, et al.
Published: (1997-01-01) -
Merosin-positive congenital muscular dystrophy: neuroimaging findings Distrofia muscular congênita merosina-positiva: achados de neuroimagem
by: André Palma da Cunha Matta, et al.
Published: (2007-03-01) -
Avaliação da função motora em crianças com distrofia muscular congênita com deficiência da merosina Motor function evaluation in merosin-deficient congenital muscular dystrophy children
by: Fernanda M. Rocco, et al.
Published: (2005-06-01) -
Dystrophin-glycoproteins associated in congenital muscular dystrophy: immunohistochemical analysis of 59 Brazilian cases Complexo distrofina-glicoproteínas associadas na distrofia muscular congênita: análise imuno-histoquímica em 59 casos
by: Lucio Gobbo Ferreira, et al.
Published: (2005-09-01)