Mild skeletal muscle symptoms might be accompanied with severe cardiac disease, sometimes indicating a serious inherited disorder. Very often it is a cardiologist who refers a patient with cardiomyopathy and/or cardiac arrhythmia and discrete muscle disease for neurological consultation, which helps to establish a proper diagnosis. Here we present three families in which a diagnosis of skeletal muscle laminopathy was made after careful examination of the members, who presented with cardiac arrhythmia and/or heart failure and a mild skeletal muscle disease, which together with positive family history allowed to direct the molecular diagnostics and then provide appropriate treatment and counseling
BACKGROUND AND PURPOSE: The early diagnosis of LMNA-associated muscular dystrophy is important for p...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...
Mild skeletal muscle symptoms might be accompanied with severe cardiac disease, sometimes indicating...
Mutations in the LMNA gene are associated with a wide spectrum of disease phenotypes, ranging from n...
Skeletal muscle channelopathies are a group of rare episodic genetic disorders comprising the period...
Skeletal muscle channelopathies are a group of rare episodic genetic disorders comprising the period...
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
Muscular dystrophy (MD) connotes a heterogeneous group of inherited disorders characterized by progr...
This study was performed to evaluate the characteristics, mode of inheritance and etiology of famili...
Emery-Dreifuss muscular dystrophy (EDMD) is characterized by early-onset contractures, slowly progre...
Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscu...
LMNA-related disorders are caused by mutations in the LMNA gene, which encodes for the nuclear envel...
Mutations in lamins, which are ubiquitous nuclear intermediate filaments, lead to a variety of disor...
SummaryInherited cardiomyopathies may arise from mutations in genes that are normally expressed in b...
BACKGROUND AND PURPOSE: The early diagnosis of LMNA-associated muscular dystrophy is important for p...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...
Mild skeletal muscle symptoms might be accompanied with severe cardiac disease, sometimes indicating...
Mutations in the LMNA gene are associated with a wide spectrum of disease phenotypes, ranging from n...
Skeletal muscle channelopathies are a group of rare episodic genetic disorders comprising the period...
Skeletal muscle channelopathies are a group of rare episodic genetic disorders comprising the period...
Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical fe...
Muscular dystrophy (MD) connotes a heterogeneous group of inherited disorders characterized by progr...
This study was performed to evaluate the characteristics, mode of inheritance and etiology of famili...
Emery-Dreifuss muscular dystrophy (EDMD) is characterized by early-onset contractures, slowly progre...
Cardiac disease is a common clinical manifestation of neuromuscular disorders, particularly of muscu...
LMNA-related disorders are caused by mutations in the LMNA gene, which encodes for the nuclear envel...
Mutations in lamins, which are ubiquitous nuclear intermediate filaments, lead to a variety of disor...
SummaryInherited cardiomyopathies may arise from mutations in genes that are normally expressed in b...
BACKGROUND AND PURPOSE: The early diagnosis of LMNA-associated muscular dystrophy is important for p...
The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting ...
Diseases of muscle may be congenital or acquired. They cause muscle weakness without sensory loss. T...