Introduction: Limb girdle weakness is one of the frequent clinical diagnoses in neurological clinics. Their etiology, treatment and prognosis are varied in different geographical regions of the world. Materials and methods: Patient cohort of 68 patients with limb girdle weakness from a tertiary hospital in South India were studied. Results: Most of the patients were found to have muscular dystrophies with LGMD variety being the highest reported. Out of 48 cases of muscle disorders LGMD [17/48] and DMD [14/48] formed the majority. Very few of them had a family history and they had little evidence of cardiac involvement. Males were more affected in DMD and BMD. LGMD males outnumbered female patients in this study. Conclusion: Our study report...
The increasing knowledge about limb girdle muscular dystrophy (LGMD) has clarified many aspects of t...
OBJECTIVE: To determine the clinical spectrum of limb-girdle muscular dystrophy 2E (LGMD2E) and to i...
Limb girdle muscular dystrophies are heterogeneous autosomal hereditary neuromuscular disorders. The...
The clinical syndrome of slowly progressive proximal limb and limb girdle muscular weakness and atro...
Introduction: Limb-girdle muscular dystrophy refers to disorders that cause wasting and weakness of ...
This first description of the oculopharyngeal muscular dystrophy (OPMD) phenotype in Dutch patients ...
Limb girdle muscular dystrophies (LGMD) encompass inherited muscle disorders that are named after th...
Limb-girdle muscular dystrophies (LGMDs) and distal dystrophies are a diverse group of genetically h...
Background: The term limb girdle muscular dystrophy (LGMD) describes a group of genetic muscular dis...
Objective: To review the current evidence and make practice recommendations regarding the diagnosis ...
Introduction: Limb girdle muscular dystrophies (LGMDs) are characterized by high molecular heterogen...
A cross-sectional study was performed in the Netherlands to define the clinical characteristics of t...
Limb girdle muscular dystrophies (LGMD) are characterized by involvement of the pelvic and shoulder ...
This study determined the frequency and impact of symptoms on quality of life in patients diagnosed ...
Objective: To evaluate the reliability and accuracy of skeletal muscle CT to correctly identify diff...
The increasing knowledge about limb girdle muscular dystrophy (LGMD) has clarified many aspects of t...
OBJECTIVE: To determine the clinical spectrum of limb-girdle muscular dystrophy 2E (LGMD2E) and to i...
Limb girdle muscular dystrophies are heterogeneous autosomal hereditary neuromuscular disorders. The...
The clinical syndrome of slowly progressive proximal limb and limb girdle muscular weakness and atro...
Introduction: Limb-girdle muscular dystrophy refers to disorders that cause wasting and weakness of ...
This first description of the oculopharyngeal muscular dystrophy (OPMD) phenotype in Dutch patients ...
Limb girdle muscular dystrophies (LGMD) encompass inherited muscle disorders that are named after th...
Limb-girdle muscular dystrophies (LGMDs) and distal dystrophies are a diverse group of genetically h...
Background: The term limb girdle muscular dystrophy (LGMD) describes a group of genetic muscular dis...
Objective: To review the current evidence and make practice recommendations regarding the diagnosis ...
Introduction: Limb girdle muscular dystrophies (LGMDs) are characterized by high molecular heterogen...
A cross-sectional study was performed in the Netherlands to define the clinical characteristics of t...
Limb girdle muscular dystrophies (LGMD) are characterized by involvement of the pelvic and shoulder ...
This study determined the frequency and impact of symptoms on quality of life in patients diagnosed ...
Objective: To evaluate the reliability and accuracy of skeletal muscle CT to correctly identify diff...
The increasing knowledge about limb girdle muscular dystrophy (LGMD) has clarified many aspects of t...
OBJECTIVE: To determine the clinical spectrum of limb-girdle muscular dystrophy 2E (LGMD2E) and to i...
Limb girdle muscular dystrophies are heterogeneous autosomal hereditary neuromuscular disorders. The...