Twenty five patients with sarcoglycanopathies were studied prospectively. 21 of them had mild phenotype. Muscle involvement was more pronounced in adductor and flexor groups of muscles of the limbs, hip adductor muscles being the weakest. The selective and differential weakness between weak hip adductors and stronger hip abductors resulted in the hip abduction sign in 64% of cases. Distal muscle involvement in lower limbs was seen in 92% of cases, but was mild and late in the course of the disease. 44% patients had winging of scapulae. Immunocytochemistry showed multiple sarcoglycan deficiencies in 84% patients. Primary β and δ sarcoglycanopathy was seen in the remaining 16% cases. Secondary dystrophin reduction was seen in 44% patients and...
Sarcoglycanopathies constitute a subgroup of limb-girdle recessive muscular dystrophies due to defec...
Objectives To characterise the pattern and spectrum of involvement on muscle MRI in a large cohort o...
Sarcoglycanopathies include four subtypes of autosomal recessive limb-girdle muscular dystrophies (L...
Background: Sarcoglycanopathies are a group or autosomal recessive muscular dystrophies designated a...
BACKGROUND: Limb girdle muscular dystrophy (LGMD) is a phenotypic expression of a heterogeneous grou...
International audienceSarcoglycanopathies are the third most common cause of autosomal recessive lim...
Introduction: By reviewing the literature from the last twenty years we present an accurate assessme...
Background : Limb girdle muscular dystrophy (LGMD) is a heterogeneous group of disorders characteriz...
INTRODUCTION: Limb-girdle muscular dystrophy presents with heterogeneous clinical and molecular feat...
A group of 204 muscular dystrophy patients were screened for immunohistochemical and biochemical alp...
OBJECTIVES: To characterise the pattern and spectrum of involvement on muscle MRI in a large cohort ...
Patients with sarcoglycanopathies, which comprise four subtypes of autosomal recessive limb-girdle m...
Sarcoglycanopathies constitute a subgroup of limb-girdle recessive muscular dystrophies due to defec...
Objectives To characterise the pattern and spectrum of involvement on muscle MRI in a large cohort o...
Sarcoglycanopathies include four subtypes of autosomal recessive limb-girdle muscular dystrophies (L...
Background: Sarcoglycanopathies are a group or autosomal recessive muscular dystrophies designated a...
BACKGROUND: Limb girdle muscular dystrophy (LGMD) is a phenotypic expression of a heterogeneous grou...
International audienceSarcoglycanopathies are the third most common cause of autosomal recessive lim...
Introduction: By reviewing the literature from the last twenty years we present an accurate assessme...
Background : Limb girdle muscular dystrophy (LGMD) is a heterogeneous group of disorders characteriz...
INTRODUCTION: Limb-girdle muscular dystrophy presents with heterogeneous clinical and molecular feat...
A group of 204 muscular dystrophy patients were screened for immunohistochemical and biochemical alp...
OBJECTIVES: To characterise the pattern and spectrum of involvement on muscle MRI in a large cohort ...
Patients with sarcoglycanopathies, which comprise four subtypes of autosomal recessive limb-girdle m...
Sarcoglycanopathies constitute a subgroup of limb-girdle recessive muscular dystrophies due to defec...
Objectives To characterise the pattern and spectrum of involvement on muscle MRI in a large cohort o...
Sarcoglycanopathies include four subtypes of autosomal recessive limb-girdle muscular dystrophies (L...